Forensic biology

Last updated

Forensic biology involves the application of biological principles and techniques within the context of law enforcement investigations. [1] [2]

Contents

Forensic biology primary focuses on DNA sequencing of biological matter discovered at crime scenes, [3] aiding investigators in identifying potential suspects or unidentified bodies. This field encompasses various sub-branches, including forensic anthropology, forensic entomology, forensic odontology, forensic pathology, and forensic toxicology.

Disciplines

History

The first recorded use of forensic procedures dates back to the 7th century when the concept of using fingerprints as a means of identification was first established. [4]

By the end of the 7th century, forensic procedures were being used to ascertain the guilt of criminals, among other purposes. [5] [6]

One of the early pioneers in employing these methods, which would later evolve into the field of forensics, was Alphonse Bertillon, also known as the "father of criminal identification". [7] In 1879, he introduced a scientific approach to personal identification by developing the science of anthropometry. [8] [9] [10] This method involved a series of body measurements for distinguishing one human individual from another.

Karl Landsteiner later made further significant discoveries in forensics. [11] In 1901, he was the first to categorise human blood into different groups: A, B, AB, and O, [12] and thus blood typing was introduced to the world of crime-solving. [13]

Dr Leone Lattes, a professor at the Institute of Forensic Medicine in Turin, Italy, [14] [15] is another to have made significant contributions to forensics. In 1915, he discovered a method to determine the blood group of dried bloodstains, a significant advancement from prior techniques limited to analysing liquid blood. This technique was subsequently adopted for criminal investigation. [16] [17]

In 1928, Albrecht. H.O, a German chemist, developed a chemical solution called luminol, which can be used to detect trace amounts of blood stains at crime scenes. [18] [19]

Among others, Sir Alec Jeffreys contributed further to modern forensics. In 1984, he developed the DNA fingerprinting technique to examine the variations in the genetic code. This can be used to distinguish one individual from another. This method has become important in forensic science to assist police detective work, and it has also proved useful in resolving paternity and immigration disputes. [20]

In 1983, Kary B. Mullis made a significant contribution to the fields of medicine and criminology by developing the PCR (polymerase chain reaction) technique, which can amplify even trace amount of DNA segments in-vitro. [21] Such DNA samples, often found in crime scenes in minute amounts, degraded states and sometimes mixed with various body fluids from multiple individuals, can be effectively amplified using PCR. Beyond forensics, PCR has been applied to a wide range of fields, including disease diagnosis and virus detection. [22]

DNA analysis

DNA, or deoxyribonucleic acid, is one of the most popular pieces of evidence to recover at a crime scene. [23] More often than not, evidence containing DNA is regarded as biological evidence . [24] With all of the substantial advances that have been made regarding DNA, biological evidence is recognized to be the "golden standard" in forensic science. [25] [26]

At the scene, biological evidence must be initially visibly recognized. Sometimes this is not always possible and the aid of an alternative light source, or Advanced Light Source (ALS), is required. [27] [28] Once identified as a potential source, presumptive tests are conducted to establish the possibility of the specified biological presence (semen, saliva, blood, urine, etc.). [23] If positive, samples are collected and submitted for analysis in the laboratory, where confirmatory tests and further tests are performed. [2] [23]

DNA analysis has numerous applications, such as paternity testing, identification of unknown human remains, breakthroughs in cold cases, as well as connecting suspects and/or victims to a piece (or pieces) of evidence, a scene, or another person (either a victim or suspect). [23] [29] [30] [31] Nuclear DNA evidence can be recovered from blood, semen, saliva, epithelial cells and hair (provided the root is still intact). [23] Furthermore, Mitochondrial DNA (mtDNA) can be recovered from the shaft of hair, bone, and the roots of teeth.

For most forensic DNA samples, STR analysis of autosomal short tandem repeats (STR) is performed in an attempt to individualize the sample to one person with a high degree of statistical confidence. [32] [33] [34] [35] Here, STR markers for autosomal STR are used in forensic DNA typing to track down the missing, verify family connections, and potentially connect suspects to crime sites. [36]

TaqMan Probes TaqMan Probes.jpg
TaqMan Probes
STR electropherogram of a three-person mixture STR electropherogram of a three person mixture.jpg
STR electropherogram of a three-person mixture

Laboratory analysis of DNA evidence involves the sample DNA being extracted, quantified, amplified, and visualized. There are several methods of DNA extraction possible including organic (phenol-chloroform) extraction, Chelex extraction, [37] and differential extraction.

Quantitation is commonly conducted using a form of the polymerase chain reaction, known as real-time PCR, quantitative PCR (qPCR). [38] [39] qPCR is the preferred method of DNA quantitation for forensic cases because it is very precise, human-specific, qualitative, and quantitative. [40] [41] This technique analyses changes in fluorescence signals of amplified DNA fragments between each PCR cycle without needing to pause the reaction or open the temperature-sensitive PCR tubes. [40] In addition to the components necessary for standard a PCR reaction (i.e. template DNA, carefully designed forward and reverse primers, DNA polymerase [usually Taq ], dNTPs, and a buffer solution containing Mg2+), qPCR reactions involve fluorescent dye-labelled probes that complement and anneal to the DNA sequence of interest that lies between the two primers. [40] A "reporter" (R) dye is attached at the 5’ end of the fluorescent probe, while a "quencher" (Q) dye is attached at the 3’ end. Before the DNA strands are extended by the polymerase, the reporter and quencher are close enough in space that no fluorescence is detected by the instrument (the quencher completely absorbs/masks the fluorescence of the reporter). As the polymerase begins to extend the strand, the 5' end of the probe is degraded by the polymerase due to its exonuclease activity. The reporter dye is released from the 5’ end. It is no longer quenched, thus enabling fluorescence detection. [38] [39] A graph is constructed for the sample DNA comparing the presence of fluorescence (y-axis) to cycle number (x-axis) of the qPCR process. This is then compared to a standard curve of the cycle fluorescence threshold (y-axis) versus the log of known DNA concentrations (x-axis). [42] By comparing the sample data to the standard curve, one may extrapolate the DNA concentration in the sample, which is essential to move forward with PCR amplification and capillary electrophoresis to obtain a DNA profile. DNA profiles are produced as an electropherogram. The obtained profile can be compared to known samples in CODIS to identify a possible suspect. [2] Based on known frequencies of the genotype found in the DNA profile, the DNA analyst may place a statistical measure of confidence on DNA match. [43]

Mitochondrial DNA analysis

Mitochondrial DNA (mtDNA) is used [44] instead of nuclear DNA when forensic samples have been degraded, are damaged, or are in very small quantities. In many cases, there may be older human remains, sometimes ancient, and the only options for DNA collection are the body's bone, teeth, or hair. [45]

mtDNA can be extracted from such degraded samples since its presence in cells is much higher than nuclear DNA. There can be more than 1,000 copies of mtDNA in a cell, [46] while there are only two copies of nuclear DNA. [45] Nuclear DNA is inherited from both the mother and the father but mtDNA is passed down from only the mother to all of her offspring. [47] [45] Due to this type of inheritance, mtDNA is useful for identification purposes in forensic work but can also be used for mass disasters, missing persons cases, complex kinship, and genetic genealogy. [45]

The main advantage of using mtDNA is its high copy number. [48] However, there are a few disadvantages of using mtDNA as opposed to nuclear DNA. Since mtDNA is inherited maternally and passed to each offspring, all members of the maternal familial line will share a haplotype. [49] A haplotype "is a group of alleles in an organism that are inherited together from a single parent". Sharing this haplotype among family members can cause an issue in forensic samples because these samples are often mixtures that contain more than one DNA contributor. [45] De convolution and interpretation of mtDNA mixtures is more difficult than that of nuclear DNA, and some laboratories choose not to attempt the process [50] Since mtDNA does not recombine, the genetic markers are not as diverse as autosomal STRs are in the case of nuclear DNA. [49] Another issue is that of heteroplasmy — when an individual has more than one type of mtDNA in their cells. [45] This can cause an issue in interpreting data from questioned forensic samples and known samples that contain mtDNA. [51] Having adequate knowledge and understanding of heteroplasmy can help ensure successful interpretation. [51]

There are some ways to improve success of mtDNA analysis. Preventing contamination at all testing stages and using positive and negative controls is a priority. [45] In addition, the use of mini-amplicons can be beneficial. When a sample of mtDNA is severely degraded or has been obtained from an ancient source, the use of small amplicons can be used to improve the success of amplification during PCR. [45] In these cases primers amplifying smaller regions of HV1 and HV2 in the control region of mtDNA are used. [52] This process has been referred to as the 'ancient DNA' approach. [45]

The first use of mtDNA as evidence in court was in 1996 in State of Tennessee v. Paul Ware. [53] [54] There was only circumstantial evidence against Ware so the admittance of mtDNA from hairs found in the victim's throat and at the scene were key to the case. [54]

In 2004, with the help of the National Center for Missing and Exploited Children and ChoicePoint, mtDNA was used to solve a 22-year-old cold case where the nuclear DNA evidence was not originally strong enough. [55] After mtDNA analysis, Arbie Dean Williams was convicted of the murder of 15-year-old Linda Strait, which had occurred in 1982. [55] [56]

In 2012, mtDNA evidence allowed investigators to establish a link in a 36-year-old investigation into the murders of four Michigan children. [57] Hair fibers found on the bodies of two of the children were tested and the mtDNA found to be the same for each sample. For the investigators this was a big break because it meant that the murders were likely connected. [57]

Forensic anthropology

Anthropology is applied to forensics most regularly through the collection and analysis of human skeletal remains. [2] [58] [59] The primary goals of anthropological involvement include identification and aiding in scene reconstruction by determining details regarding the circumstances of the victim's death. In cases where conventional techniques [60] are unable to determine the identity of the remains due to the lack of soft tissue, anthropologists are required to deduce certain characteristics based on the skeletal remains. Race, sex, age and possible ailments can often be determined through bone measurements and looking for clues throughout the skeletal structure.

This becomes necessary when conventional methods that use soft tissue [60] fail to establish the identity of remains. By examining bone measurements and other skeletal structure characteristics, anthropologists can often determine information such as race, sex, age, and potential health conditions.

Forensic botany

Forensic botany deals with the study of plants, leaves, seeds, and pollen or plant properties (such as anatomy, growth, behavior, classification, population dynamics, and reproductive cycles) that would be considered as physical evidence. [61] [62]

Before a plant can aid the investigations, the plant must be identified first to see if it is from the location that the plant was found. Forensic botany can help investigators by providing a link between an individual and the crime scene by pinpointing the geographical location of missing bodies or estimate where the burial took place. Another way that is used is through the interrogation process where investigators compare the traces that the victim(s) are found and compare to the statements of the suspect(s). [63] Forensic botany can also reveal whether a death is due to suicide, accident, or homicide. Another example of forensic botany aiding investigators is by moss, moss can establish the PMI of a human skeletal, through its growth rate. [64]

For example, an elderly man fell a steep hillside and was found dead. They concluded that the man did not die from the fall but from hypertensive heart disease. Forensic botany concluded that the fall was approximately 10 m and there was a lane that joined the hill path around 9 m perpendicular form the body. It showed he had leaves on his left hand and sweater. There were also broken bushes in the scene. Forensic scientists specializing in forensic botany had grabbed five soil samples and some plant samples from the scene. The plant samples were analyzed through optical microscopy, and they also examined the victims' clothing since it did carry some plant elements. They did a macroscopic and microscopic analysis compared to the collected samples on the scene. It was concluded that there was no evidence of struggle caused by another person instead, the elderly man had lost his balance. [63]

Subspecialties In Forensic Botany

Subdisciplines within forensic botany examples include:

Forensic ornithology

Forensic ornithology employs scientific methodologies to ascertain the bird species from traces of evidence such as a small feather, a fragment of bone, or a trace of blood. [66] Bird remains can be identified, first and foremost from feathers as feathers exhibit distinctive characteristics specific to a particular bird species, which can be observed both at a macroscopic and microscopic level.

Forensic odontology

Dentistry has helped law enforcement detect and solve cases in criminal and civil proceedings. Odontology did not get popular until the 1960s when an interest was brought up by the first instructional program in the United States at the Armed Forces Institute of Pathology. As a result of this program, the term "forensic odontology" is now widely known and understood by both dental and law enforcement professionals.

Odontologists or dental professionals can use dental science to establish a person's identity. The broad duties of a Forensic Odontologist include forensic identification of individuals, including in multi-casualty events, age estimation in living and deceased persons, interpreting injuries in the oral and perioral regions, bite mark analysis and comparison, and assisting forensic pathologists in determining the cause of death if there is a possible contributing dental condition. [67]

Dental evidence is useful in establishing human identity by comparing the dental features of a deceased person with antemortem dental records. [68]

Forensic pathology

Forensic pathology is a subfield in forensics where experts examine persons (bodies) who die suddenly, unexpectedly or violently, and thus determine the cause of death. [69] The function of a forensic autopsy is to provide information through a postmortem examination of the body and analysis of the fluids to determine the cause of death, manner of death, and mechanism of injury. [70]

A forensic pathologist is a medical doctor who is an expert in both trauma and disease and is responsible for performing autopsies. He/she applies their extensive knowledge of the human body and possible internal and external inflections as he/she performs an autopsy, to ascertain the manner and cause of death hopefully. [2]

Information derived from the autopsy often greatly assists investigative efforts and scene reconstruction.

Forensic toxicology

Forensic toxicology is the use of toxicology and other disciplines such as analytical chemistry, pharmacology and clinical chemistry to aid medical or legal investigation of death, poisoning, and drug use. The primary concern for forensic toxicology is not the legal outcome of the toxicological investigation or the technology utilized but rather the obtainment and interpretation of results.

Forensic microbiology

With recent advances in massive parallel sequencing (MPS), or next-generation sequencing (NGS), forensic microbiology has become an increasingly promising area of research. "Initial applications in circumstances of biocrime, bioterrorism and epidemiology use microorganisms for the following reasons: (i) as ancillary evidence in criminal cases; (ii) to clarify causes of death (e.g., drownings, toxicology, hospital-acquired infections, sudden infant death and shaken baby syndromes); (iii) to assist human identification (skin, hair and body fluid microbiomes); (iv) for geolocation (soil microbiome or microbiome of bodies of water); and (v) to estimate postmortem interval (PMI) via thanatomicrobiome [71] [72] and epinecrotic [73] [74] microbial community". [75] In fact, scientists estimate the time elapsed since death or the PMI by analyzing the stage of decay from bacterial decomposition [74] or the bacterial succession patterns.

Bioterrorism and epidemiology

Bio terrorism occurs when biological components are used as warfare agents. Such biological weapons are microorganisms that are deliberately dispersed to incapacitate or cause disease and death to humans, animals or plants. Biological warfare agents can be natural or genetically modified. [76] Nevertheless, these biological agents - be it viruses, bacteria or fungi are highly contagious.

Forensic microbiology also contributes to the development of epidemiology. By examining microorganisms obtained from infected individuals, scientists can determine a suspected source of infection, the type of infection present, and the evolution or mutation pattern of the microorganism. The application of a forensic microbiologist would be to examine the microorganisms isolated from infected individuals and compare it to known sources of infectious pathogens. [77]

"It is important to remember that biological agents that can be used as weapons are often found in the environment. For this reason, it is always difficult to determine whether infections associated with these bioagents are accidental or purposely started". [75] While not the first, or only, incidence of bioterrorism, perhaps the most notable case in recent memory involved the sending of at least four anthrax-containing envelopes in the United States in September and October 2001. "At least 22 victims contracted anthrax due to the mailings: 11 individuals contracted inhalation anthrax, with 5 of these infections resulting in fatalities; another 11 individuals suffered cutaneous anthrax. In addition, 31 persons tested positive for exposure to B. anthracis spores". [78] However, the advancements in PCR and whole-genome sequencing allowed scientists to collaborate with the FBI and identify the source of the letter spores.

Differentiating a biowarfare attack from a normal epidemiology outbreak

The basic epidemiologic approach to evaluating a potential bioterrorist or biowarfare attack differs from any standard epidemiologic investigation. The first step uses laboratory and clinical findings to confirm that a disease outbreak has occurred. Once the case definition and attack rate have been determined, the outbreak can be characterized in the conventional context of time, place, and person. These data provide crucial information in determining the potential source of the outbreak. An epidemic curve can be calculated using data gathered on cases over time. The disease pattern is important to differentiate between a natural outbreak and an intentional attack. A bioterrorism attack is most likely caused by a point source, with everyone coming in contact with the agent at approximately the same time. Additional characteristics investigated in determining whether it is the result of a biological attack are: the presence of a large epidemic; more severe disease than expected for a given pathogen; a disease that is unusual for a given geographic area; and multiple simultaneous epidemics of different diseases. [79]

Postmortem analysis

"Post-mortem microbiology (PMM) aims to detect unexpected infections causing sudden deaths; confirm clinically suspected but unproven infection; evaluate the efficacy of antimicrobial therapy; identify emergent pathogens; and recognize medical errors. Additionally, the analysis of the thanatomicrobiome may help to estimate the post-mortem interval.". [80] There is currently an extensive amount of research being performed, most notably using the famous "body farms" throughout the United States, to determine if there is a consistent microbial decomposition "clock" that could be used by itself, or in conjunction with other techniques (such as forensic entomology) to help estimate postmortem intervals. One such group has made extensive headway into describing such a microbial clock, and "believes she's within two to five years of testing her clock in a real crime scene scenario". [81] However, if a reliable and consistent microbial clock is determined to exist, "it's too soon to know whether the microbial clock will pass scientific and legal muster," (Beans) and "a judge would also have to determine that the microbial clock meets the standard for admission of expert testimony". [81]

Water sample analysis

In cases involving a body of water at or near the scene of a crime, a sample of the water can be extracted and analyzed under a light microscope for microorganisms. One such microorganism that are analyzed within samples of fresh water are diatoms, microscopic algae of varying shapes. Different bodies of water have been found to contain unique sets of diatoms and therefore, a piece of evidence found in a specific body of water will contain unique diatoms on it found only in that specific body of water. Therefore, the diatoms on a questioned object or body can be compared to the diatoms from a body of water to determine whether it had been present in the water. [82]

Current issues

Sexual assault kit backlog

Prior to DNA testing, many sexual assault cases could only rely on "he said, she said" and possible witnesses. Even once DNA analysis was available, many sexual assault kits, or SAKs, were never tested and thrown into a backroom or storage facility, only to be forgotten until discovered. Since DNA analysis is frequently utilized in most cases, most SAKs are examined and analyzed. However, the issue remains about the preexisting SAKs that have never been tested. A prevalent issue then, that still extends to now, is the absence of funds to process and analyze these SAKs. Many districts would dedicate their funds to homicides or more high-profile cases and sexual assaults would be swept aside. The biggest concern about all of these SAKs, is how to go about processing all of them, especially as more and more are being found each year. [83]

Cold cases

With the considerable advances in DNA analysis, old, open cases with intact evidence can be examined for biological evidence. [32] New profiles are uploaded to CODIS every day so the base population to search and compare to increases. Biological testing for cold cases, specifically homicides, encounters similar roadblocks as the SAKs - lack of funds or the DNA samples have not been properly stored; thus too much degradation has occurred for viable analyses.

In popular culture, forensic biology is frequently portrayed in shows like Law & Order , Hannibal, Bones , CSI , Dexter and Castle . However thanks to Hollywood's depiction of forensic science, the analysis of biological evidence has fallen prey to the CSI Effect, which results in the public's perception of its capabilities being severely distorted and its limits blurred.

See also

Related Research Articles

<span class="mw-page-title-main">Polymerase chain reaction</span> Laboratory technique to multiply a DNA sample for study

The polymerase chain reaction (PCR) is a method widely used to make millions to billions of copies of a specific DNA sample rapidly, allowing scientists to amplify a very small sample of DNA sufficiently to enable detailed study. PCR was invented in 1983 by American biochemist Kary Mullis at Cetus Corporation. Mullis and biochemist Michael Smith, who had developed other essential ways of manipulating DNA, were jointly awarded the Nobel Prize in Chemistry in 1993.

A microsatellite is a tract of repetitive DNA in which certain DNA motifs are repeated, typically 5–50 times. Microsatellites occur at thousands of locations within an organism's genome. They have a higher mutation rate than other areas of DNA leading to high genetic diversity. Microsatellites are often referred to as short tandem repeats (STRs) by forensic geneticists and in genetic genealogy, or as simple sequence repeats (SSRs) by plant geneticists.

<span class="mw-page-title-main">DNA profiling</span> Technique used to identify individuals via DNA characteristics

DNA profiling is the process of determining an individual's deoxyribonucleic acid (DNA) characteristics. DNA analysis intended to identify a species, rather than an individual, is called DNA barcoding.

<span class="mw-page-title-main">Forensic palynology</span> Forensic application of the study of particulate matter

Forensic palynology is a subdiscipline of palynology, that aims to prove or disprove a relationship among objects, people, and places that may pertain to both criminal and civil cases. Pollen can reveal where a person or object has been, because regions of the world, countries, and even different parts of a single garden will have a distinctive pollen assemblage. Pollen evidence can also reveal the season in which a particular object picked up the pollen. Recent research into forensic palynology has seen advancements in DNA barcoding from pollen, to the level of singular pollen molecules, allowing DNA profiles to be created from singular palynomorphs, streamlining the efficiency and accuracy of taxonomic identification.

Archaeogenetics is the study of ancient DNA using various molecular genetic methods and DNA resources. This form of genetic analysis can be applied to human, animal, and plant specimens. Ancient DNA can be extracted from various fossilized specimens including bones, eggshells, and artificially preserved tissues in human and animal specimens. In plants, ancient DNA can be extracted from seeds and tissue. Archaeogenetics provides us with genetic evidence of ancient population group migrations, domestication events, and plant and animal evolution. The ancient DNA cross referenced with the DNA of relative modern genetic populations allows researchers to run comparison studies that provide a more complete analysis when ancient DNA is compromised.

<span class="mw-page-title-main">Forensic dentistry</span> Aspect of criminal investigation

Forensic dentistry or forensic odontology involves the handling, examination, and evaluation of dental evidence in a criminal justice context. Forensic dentistry is used in both criminal and civil law. Forensic dentists assist investigative agencies in identifying human remains, particularly in cases when identifying information is otherwise scarce or nonexistent—for instance, identifying burn victims by consulting the victim's dental records. Forensic dentists may also be asked to assist in determining the age, race, occupation, previous dental history, and socioeconomic status of unidentified human beings.

Forensic identification is the application of forensic science, or "forensics", and technology to identify specific objects from the trace evidence they leave, often at a crime scene or the scene of an accident. Forensic means "for the courts".

<span class="mw-page-title-main">STR analysis</span> Biological DNA analysis for allele repeats

Shorttandemrepeat (STR) analysis is a common molecular biology method used to compare allele repeats at specific loci in DNA between two or more samples. A short tandem repeat is a microsatellite with repeat units that are 2 to 7 base pairs in length, with the number of repeats varying among individuals, making STRs effective for human identification purposes. This method differs from restriction fragment length polymorphism analysis (RFLP) since STR analysis does not cut the DNA with restriction enzymes. Instead, polymerase chain reaction (PCR) is employed to discover the lengths of the short tandem repeats based on the length of the PCR product.

A DNA database or DNA databank is a database of DNA profiles which can be used in the analysis of genetic diseases, genetic fingerprinting for criminology, or genetic genealogy. DNA databases may be public or private, the largest ones being national DNA databases.

<span class="mw-page-title-main">Use of DNA in forensic entomology</span>

Forensic entomology has three sub-fields: urban, stored product and medico-criminal entomologies. This article focuses on medico-criminal entomology and how DNA is analyzed with various blood-feeding insects.

<span class="mw-page-title-main">Body identification</span> Subfield of forensic science

Body identification is a subfield of forensic science that uses a variety of scientific and non-scientific methods to identify a body. Forensic purposes are served by rigorous scientific forensic identification techniques, but these are generally preceded by formal identification. This involves requesting a family member or friend of the victim to visually identify the body.

Multiple displacement amplification (MDA) is a DNA amplification technique. This method can rapidly amplify minute amounts of DNA samples to a reasonable quantity for genomic analysis. The reaction starts by annealing random hexamer primers to the template: DNA synthesis is carried out by a high fidelity enzyme, preferentially Φ29 DNA polymerase. Compared with conventional PCR amplification techniques, MDA does not employ sequence-specific primers but amplifies all DNA, generates larger-sized products with a lower error frequency, and works at a constant temperature. MDA has been actively used in whole genome amplification (WGA) and is a promising method for application to single cell genome sequencing and sequencing-based genetic studies.

Rape investigation is the procedure to gather facts about a suspected rape, including forensic identification of a perpetrator, type of rape and other details.

Touch DNA, also known as Trace DNA, is a forensic method for analyzing DNA left at the scene of a crime. It is called "touch DNA" because it only requires very small samples, for example from the skin cells left on an object after it has been touched or casually handled, or from footprints. Touch DNA analysis only requires seven or eight cells from the outermost layer of human skin. The technique has been criticized for high rates of false positives due to contamination—for example, fingerprint brushes used by crime scene investigators can transfer trace amounts of skin cells from one surface to another, leading to inaccurate results. Because of the risk of false positives, it is more often used by the defense to help exclude a suspect rather than the prosecution.

Forensic serology is the detection, identification, classification, and study of various bodily fluids such as blood, semen, saliva, and urine, and their relationship to a crime scene. A forensic serologist may also be involved in DNA analysis and bloodstain pattern analysis. Serology testing begins with presumptive tests which gives the analyst an indication that a specific bodily fluid may be present, but cannot completely confirm its presence. Following the presumptive tests, confirmatory tests are done on the same sample to confirm what the unknown substance actually is.

In paternity testing, Paternity Index (PI) is a calculated value generated for a single genetic marker or locus and is associated with the statistical strength or weight of that locus in favor of or against parentage given the phenotypes of the tested participants and the inheritance scenario. Phenotype typically refers to physical characteristics such as body plan, color, behavior, etc. in organisms. However, the term used in the area of DNA paternity testing refers to what is observed directly in the laboratory. Laboratories involved in parentage testing and other fields of human identity employ genetic testing panels that contain a battery of loci each of which is selected due to extensive allelic variations within and between populations. These genetic variations are not assumed to bestow physical and/or behavioral attributes to the person carrying the allelic arrangement(s) and therefore are not subject to selective pressure and follow Hardy Weinberg inheritance patterns.

<span class="mw-page-title-main">DNA barcoding</span> Method of species identification using a short section of DNA

DNA barcoding is a method of species identification using a short section of DNA from a specific gene or genes. The premise of DNA barcoding is that by comparison with a reference library of such DNA sections, an individual sequence can be used to uniquely identify an organism to species, just as a supermarket scanner uses the familiar black stripes of the UPC barcode to identify an item in its stock against its reference database. These "barcodes" are sometimes used in an effort to identify unknown species or parts of an organism, simply to catalog as many taxa as possible, or to compare with traditional taxonomy in an effort to determine species boundaries.

<span class="mw-page-title-main">Wildlife forensic science</span>

Wildlife forensic science is forensic science applied to legal issues involving wildlife. Wildlife forensic sciences also deal with conservation and identification of rare species and is a useful tool for non-invasive studies. Methods can be used to determine relatedness of the animals in the area allowing them to determine rare and endangered species that are candidates for genetic rescue. Techniques using things such as the SSCP or Single-Strand Conformational Polymorphism gel electrophoresis technique, microscopy, DNA barcoding, Mitochondrial Microsatellite Analysis and some DNA and Isotope analysis can identify species and individual animals in most cases if they have already been captured. Unlike human identification, animal identification requires determination of its family, genus, and species, and sex in order to individualize the animal, typically through the use of DNA based analyses.

<span class="mw-page-title-main">DNA phenotyping</span> DNA profiling technique

DNA phenotyping is the process of predicting an organism's phenotype using only genetic information collected from genotyping or DNA sequencing. This term, also known as molecular photofitting, is primarily used to refer to the prediction of a person's physical appearance and/or biogeographic ancestry for forensic purposes.

<span class="mw-page-title-main">Forensic DNA analysis</span> Genetic analyses in crime analysis

DNA profiling is the determination of a DNA profile for legal and investigative purposes. DNA analysis methods have changed countless times over the years as technology changes and allows for more information to be determined with less starting material. Modern DNA analysis is based on the statistical calculation of the rarity of the produced profile within a population.

References

  1. "Forensic Biology | Forensic Science". forensic.unl.edu. Retrieved 2023-06-08.
  2. 1 2 3 4 5 Houck, Max; Siegal, Jay (2006). Fundamentals of Forensic Science. China: Academic Press. ISBN   978-0-12-356762-8.
  3. "Forensic Biology". www.cfsre.org. Retrieved 2023-08-31.
  4. "Origins of Forensic Science". Crime Museum. Retrieved 2023-05-31.
  5. "ORIGINS OF FORENSIC SCIENCE". CrimeMuseum.Org. Crime Museum. Retrieved 4 March 2022.
  6. admin (2017-12-29). "How Forensic Science has Evolved Over Time". IFF Lab. Retrieved 2023-05-31.
  7. lepontissalien (2019-05-04). "ALPHONSE BERTILLON: THE FATHER OF CRIMINAL IDENTIFICATION". TRACES DE FRANCE (in French). Retrieved 2023-06-08.
  8. CPHS (2020-04-07). "Criminal Identification: The Bertillon System". Cleveland Police Museum. Retrieved 2023-06-08.
  9. Tietz, Tabea (2021-04-23). "Alphonse Bertillon's Anthropometric Identification System | SciHi Blog" . Retrieved 2023-06-08.
  10. "Anthropometry | NIOSH | CDC". www.cdc.gov. 2022-09-26. Retrieved 2023-05-05.
  11. "The Nobel Prize in Physiology or Medicine 1930". NobelPrize.org. Retrieved 2023-05-05.
  12. FARHUD, Dariush D; ZARIF YEGANEH, Marjan (2013-01-01). "A Brief History of Human Blood Groups". Iranian Journal of Public Health. 42 (1): 1–6. ISSN   2251-6085. PMC   3595629 . PMID   23514954.
  13. "ABO Blood Type Identification and Forensic Science (1900-1960) | The Embryo Project Encyclopedia". embryo.asu.edu. Retrieved 2023-05-05.
  14. "Leone Lattes". prezi.com. Retrieved 2023-05-06.
  15. Staff Writer (2015-08-04). "Who Is Leone Lattes in Forensics?". Reference.com. Retrieved 2023-05-06.
  16. "Leone Lattes - Forensic's blog". forensicfield.blog. 2022-02-21. Retrieved 2023-05-06.
  17. Staff Writer (2015-08-04). "What Are Leone Lattes's Contributions to Forensic Science?". Reference.com. Retrieved 2023-05-06.
  18. Harris, Tom (2002-06-11). "How Luminol Works". HowStuffWorks. Retrieved 2023-06-08.
  19. "Luminol Test | Howtosmile". www.howtosmile.org. Retrieved 2023-06-08.
  20. "Desert Island Discs - Alec Jeffreys - BBC Sounds". www.bbc.co.uk. Retrieved 2023-05-06.
  21. "The Nobel Prize in Chemistry 1993". NobelPrize.org. Retrieved 2023-06-08.
  22. Kanojia, Shikha (11 August 2019). "Forensic Biology | Sub-Fields | Significance & Application". Science Monk.
  23. 1 2 3 4 5 Fisher, Barry A. J.; Fisher, David R. (2012). Techniques of Crime Scene Investigation. Boca Raton, Florida: CRC Press. ISBN   978-1-4398-1005-7.
  24. "Role of DNA in Forensic Science". News-Medical.net. 2021-07-09. Retrieved 2023-05-06.
  25. Hicks, T.; Coquoz, R. (2009), "Forensic DNA Evidence", in Li, Stan Z.; Jain, Anil (eds.), Encyclopedia of Biometrics, Boston, MA: Springer US, pp. 573–579, doi:10.1007/978-0-387-73003-5_106, ISBN   978-0-387-73003-5 , retrieved 2023-06-08
  26. "DNA Evidence: Basics of Identifying, Gathering and Transporting". National Institute of Justice. Retrieved 2023-05-06.
  27. "ALS Sheds a Different Light on Crime Scenes | Office of Justice Programs". www.ojp.gov. Retrieved 2023-06-08.
  28. "Alternate Light Sources | Forensics | Forensic Supplies | Sirchie". www.sirchie.com. Retrieved 2023-06-08.
  29. Butler, John M. (2015-08-05). "The future of forensic DNA analysis". Philosophical Transactions of the Royal Society B: Biological Sciences. 370 (1674): 20140252. doi:10.1098/rstb.2014.0252. ISSN   0962-8436. PMC   4580997 . PMID   26101278.
  30. Singh, Lalji (1991). "DNA profiling and its applications". Current Science. 60 (9/10): 580–585. ISSN   0011-3891. JSTOR   24099013.
  31. Saad, Rana (April 2005). "Discovery, development, and current applications of DNA identity testing". Proceedings (Baylor University. Medical Center). 18 (2): 130–133. doi:10.1080/08998280.2005.11928051. ISSN   0899-8280. PMC   1200713 . PMID   16200161.
  32. 1 2 National Institute of Justice, Office of Justice Programs (July 2002). Using DNA to Solve Cold Cases.
  33. "What Is STR Analysis?". National Institute of Justice. Retrieved 2023-06-08.
  34. Wyner, Nicole; Barash, Mark; McNevin, Dennis (2020). "Forensic Autosomal Short Tandem Repeats and Their Potential Association With Phenotype". Frontiers in Genetics. 11: 884. doi: 10.3389/fgene.2020.00884 . ISSN   1664-8021. PMC   7425049 . PMID   32849844.
  35. Nwawuba Stanley, Udogadi; Mohammed Khadija, Abdullahi; Bukola, Adams Tajudeen; Omusi Precious, Imose; Ayevbuomwan Davidson, Esewi (July 2020). "Forensic DNA Profiling: Autosomal Short Tandem Repeat as a Prominent Marker in Crime Investigation". The Malaysian Journal of Medical Sciences. 27 (4): 22–35. doi:10.21315/mjms2020.27.4.3. ISSN   1394-195X. PMC   7444828 . PMID   32863743.
  36. Keerti, Akshunna; Ninave, Sudhir; Keerti, Akshunna; Ninave, Sudhir (2022-10-12). "DNA Fingerprinting: Use of Autosomal Short Tandem Repeats in Forensic DNA Typing". Cureus. 14 (10): e30210. doi: 10.7759/cureus.30210 . ISSN   2168-8184. PMC   9650913 . PMID   36381887.
  37. Gautam, Akash (2022), Gautam, Akash (ed.), "DNA Isolation by Chelex Method", DNA and RNA Isolation Techniques for Non-Experts, Techniques in Life Science and Biomedicine for the Non-Expert, Cham: Springer International Publishing, pp. 79–84, doi:10.1007/978-3-030-94230-4_10, ISBN   978-3-030-94230-4 , retrieved 2023-06-08
  38. 1 2 Higuchi, R.; Fockler, C.; Dollinger, G.; Watson, R. (1993). "Kinetic PCR analysis: real-time monitoring of DNA amplification reactions". Bio/Technology. 11 (9): 1026–1030. doi:10.1038/nbt0993-1026. PMID   7764001. S2CID   5714001.
  39. 1 2 Higuchi, R.; Dollinger, G.; Walsh, P.S.; Griffith, R. (1992). "Simultaneous amplification and detection of specific DNA sequences". Bio/Technology. 10 (4): 413–417. doi:10.1038/nbt0492-413. PMID   1368485. S2CID   1684150.
  40. 1 2 3 Butler, John (2005). Forensic DNA Typing: Biology, Technology, and Genetics of STR Markers (2 ed.). Burlington, MA, USA: Elsevier. pp. 75–79. ISBN   978-0-12-147952-7.
  41. "Choosing the Right Method for Nucleic Acid Quantitation". www.promega.com. Retrieved 2023-06-08.
  42. Butler, John (2005). Forensic DNA Typing: Biology, Technology, and Genetics of STR Markers (2 ed.). Burlington, MA, USA: Elsevier. p. 78. ISBN   978-0-12-147952-7.
  43. Butler, John (2015). Advanced Topics in Forensic DNA Typing: Interpretation. Oxford, UK: Academic Press. pp. 213–444. ISBN   978-0-12-405213-0.
  44. Gopalakrishnan, Anupama (2015-02-25). "Mitochondrial DNA Typing in Forensics". Promega Connections. Retrieved 2023-06-08.
  45. 1 2 3 4 5 6 7 8 9 Butler, John (2005). Forensic DNA Typing: Biology, Technology, and Genetics of STR Markers, Second Edition. London, UK: Elsevier Academic Press. pp. 241–288. ISBN   978-0121479527.
  46. Zhang, Yanfang; Qu, Yiping; Gao, Ke; Yang, Qi; Shi, Bingyin; Hou, Peng; Ji, Meiju (2015-02-15). "High copy number of mitochondrial DNA (mtDNA) predicts good prognosis in glioma patients". American Journal of Cancer Research. 5 (3): 1207–1216. ISSN   2156-6976. PMC   4449448 . PMID   26045999.
  47. Luo, Shiyu; Valencia, C. Alexander; Zhang, Jinglan; Lee, Ni-Chung; Slone, Jesse; Gui, Baoheng; Wang, Xinjian; Li, Zhuo; Dell, Sarah; Brown, Jenice; Chen, Stella Maris; Chien, Yin-Hsiu; Hwu, Wuh-Liang; Fan, Pi-Chuan; Wong, Lee-Jun (2018-12-18). "Biparental Inheritance of Mitochondrial DNA in Humans". Proceedings of the National Academy of Sciences. 115 (51): 13039–13044. Bibcode:2018PNAS..11513039L. doi: 10.1073/pnas.1810946115 . ISSN   0027-8424. PMC   6304937 . PMID   30478036.
  48. Merheb, Maxime; Matar, Rachel; Hodeify, Rawad; Siddiqui, Shoib Sarwar; Vazhappilly, Cijo George; Marton, John; Azharuddin, Syed; AL Zouabi, Hussain (2019-05-09). "Mitochondrial DNA, a Powerful Tool to Decipher Ancient Human Civilization from Domestication to Music, and to Uncover Historical Murder Cases". Cells. 8 (5): 433. doi: 10.3390/cells8050433 . ISSN   2073-4409. PMC   6562384 . PMID   31075917.
  49. 1 2 Jobling, Mark A.; Gill, Peter (October 2004). "Correction: Encoded evidence: DNA in forensic analysis". Nature Reviews Genetics. 5 (10): 739–751. doi:10.1038/nrg1455. ISSN   1471-0056. PMID   15510165. S2CID   2236821.
  50. Melton, T. (July 2012). "Forensic Mitochondrial DNA Analysis: Current Practice and Future Potential" (PDF). Forensic Science Review. 24 (2): 101–22. doi:10.1201/B15361-17. PMID   26244267. S2CID   10742375. Archived from the original (PDF) on 2018-11-08. Retrieved 2018-11-08.
  51. 1 2 Melton, Terry (2004). "Mitochondrial DNA Heteroplasmy" (PDF). Forensic Science Review. 16 (1): 1–20. PMID   26256810.
  52. Erdem, S.; Altunçul, H.; Filoğlu, G.; Ölçen, A. M.; Bülbül, Ö. (2011-12-01). "Sequencing of mtDNA HV1 and HV2 regions from samples with trace amount of DNA". Forensic Science International: Genetics Supplement Series. Progress in Forensic Genetics 14. 3 (1): e455–e456. doi:10.1016/j.fsigss.2011.09.089. ISSN   1875-1768.
  53. "A New DNA Test Helps Win a Conviction". The New York Times. Associated Press. 1996-09-05. ISSN   0362-4331 . Retrieved 2023-05-06.
  54. 1 2 Davis, C. Leland (1998). "Mitochondrial DNA: State of Tennessee v. Paul Ware" (PDF). Promega. Retrieved November 5, 2018.
  55. 1 2 "DNA Profiling Helps Solve 22-year-old Murder Case". www.govtech.com. 28 July 2010. Retrieved 2018-11-07.
  56. "After 24 years, Strait murder resolved | The Spokesman-Review". www.spokesman.com. Retrieved 2023-05-06.
  57. 1 2 Boyette, Chris. "New DNA work may offer break in 36-year-old Michigan slayings". CNN. Retrieved 2018-11-07.
  58. "Forensic Anthropology | Smithsonian National Museum of Natural History". naturalhistory.si.edu. Retrieved 2023-05-06.
  59. "Forensic anthropology | science | Britannica". www.britannica.com. Retrieved 2023-05-06.
  60. 1 2 Wiersema, Jason M. (September 2016). "Evolution of Forensic Anthropological Methods of Identification". Academic Forensic Pathology. 6 (3): 361–369. doi:10.23907/2016.038. ISSN   1925-3621. PMC   6474555 . PMID   31239912.
  61. Miller Coyle, Heather, ed. (2004-09-15). Forensic Botany (0 ed.). CRC Press. doi:10.1201/9780203484593. ISBN   978-0-203-48459-3.
  62. Swetha (2020-12-26). "Forensic Botany and Its Applications". Legal Desire Media and Insights. Retrieved 2023-05-06.
  63. 1 2 Aquila, Isabella; Sacco, Matteo A.; Ricci, Pietrantonio; Gratteri, Santo (2019). "The Role of Forensic Botany in Reconstructing the Dynamics of Trauma from High Falls". Journal of Forensic Sciences. 64 (3): 920–924. doi:10.1111/1556-4029.13934. ISSN   1556-4029. PMID   30332508. S2CID   52988396.
  64. Longato, S.; Wöss, C.; Hatzer-Grubwieser, P.; Bauer, C.; Parson, W.; Unterberger, S. H.; Kuhn, V.; Pemberger, N.; Pallua, Anton K.; Recheis, W.; Lackner, R. (2015-04-07). "Post-mortem interval estimation of human skeletal remains by micro-computed tomography, mid-infrared microscopic imaging and energy dispersive X-ray mapping". Analytical Methods. 7 (7): 2917–2927. doi:10.1039/c4ay02943g. ISSN   1759-9660. PMC   4383336 . PMID   25878731.
  65. Margiotta, Gabriele; Bacaro, Giovanni; Carnevali, Eugenia; Severini, Simona; Bacci, Mauro; Gabbrielli, Mario (2015-08-01). "Forensic botany as a useful tool in the crime scene: Report of a case". Journal of Forensic and Legal Medicine. 34: 24–28. doi:10.1016/j.jflm.2015.05.003. hdl: 11368/2840167 . ISSN   1752-928X. PMID   26165654.
  66. "Solving Bird Mysteries with Forensic Ornithology - Podcast Episode". www.scienceofbirds.com. Retrieved 2023-05-06.
  67. "Forensic Odontology - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2023-05-06.
  68. "Encyclopedia of Forensic Sciences, Third Edition". ScienceDirect. Retrieved 2023-05-06.
  69. "What is a Forensic Pathologist?". hsc.unm.edu. Retrieved 2023-05-05.
  70. "Forensic Autopsy - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2023-05-06.
  71. Javan, Gulnaz T.; Finley, Sheree J. (2018-01-01), Ralebitso-Senior, T. Komang (ed.), "Chapter 6 - What Is the "Thanatomicrobiome" and What Is Its Relevance to Forensic Investigations?", Forensic Ecogenomics, Academic Press, pp. 133–143, ISBN   978-0-12-809360-3 , retrieved 2023-05-05
  72. Javan, Gulnaz T.; Finley, Sheree J.; Abidin, Zain; Mulle, Jennifer G. (2016-02-24). "The Thanatomicrobiome: A Missing Piece of the Microbial Puzzle of Death". Frontiers in Microbiology. 7: 225. doi: 10.3389/fmicb.2016.00225 . ISSN   1664-302X. PMC   4764706 . PMID   26941736.
  73. Pechal, Jennifer L.; Crippen, Tawni L.; Benbow, M. Eric; Tarone, Aaron M.; Dowd, Scot; Tomberlin, Jeffery K. (2014-01-01). "The potential use of bacterial community succession in forensics as described by high throughput metagenomic sequencing". International Journal of Legal Medicine. 128 (1): 193–205. doi:10.1007/s00414-013-0872-1. ISSN   1437-1596. PMID   23749255. S2CID   11357573.
  74. 1 2 Petkar, Tejaswini (2022-10-03). "Bacteria, Biofilms and forensic PMSI" . Retrieved 2023-05-05.
  75. 1 2 Oliveira, Manuela; Amorim, António (December 2018). "Microbial forensics: new breakthroughs and future prospects". Applied Microbiology and Biotechnology. 102 (24): 10377–10391. doi:10.1007/s00253-018-9414-6. PMC   7080133 . PMID   30302518.
  76. Roffey, R.; Lantorp, K.; Tegnell, A.; Elgh, F. (2002-08-01). "Biological weapons and bioterrorism preparedness: importance of public-health awareness and international cooperation". Clinical Microbiology and Infection. 8 (8): 522–528. doi: 10.1046/j.1469-0691.2002.00497.x . ISSN   1198-743X. PMID   12197874.
  77. Amorim, Antonio; Budowle, Bruce (2016-08-30). Handbook Of Forensic Genetics: Biodiversity And Heredity In Civil And Criminal Investigation. World Scientific. ISBN   978-1-78634-079-5.
  78. Rasko, D. A.; Worsham, P. L.; Abshire, T. G.; Stanley, S. T.; Bannan, J. D.; Wilson, M. R.; Langham, R. J.; Decker, R. S.; Jiang, L.; Read, T. D.; Phillippy, A. M.; Salzberg, S. L.; Pop, M.; Van Ert, M. N.; Kenefic, L. J.; Keim, P. S.; Fraser-Liggett, C. M.; Ravel, J. (2011-03-22). "Bacillus anthracis comparative genome analysis in support of the Amerithrax investigation". Proceedings of the National Academy of Sciences. 108 (12): 5027–5032. Bibcode:2011PNAS..108.5027R. doi: 10.1073/pnas.1016657108 . PMC   3064363 . PMID   21383169.
  79. "Epidemiology of Bioterrorism | Office of Justice Programs". www.ojp.gov. Retrieved 2023-05-31.
  80. Fernández-Rodríguez, A.; Burton, J.L.; Andreoletti, L.; Alberola, J.; Fornes, P.; Merino, I.; Martínez, M.J.; Castillo, P.; Sampaio-Maia, B.; Caldas, I.M.; Saegeman, V.; Cohen, M.C. (May 2019). "Post-mortem microbiology in sudden death: sampling protocols proposed in different clinical settings". Clinical Microbiology and Infection. 25 (5): 570–579. doi: 10.1016/j.cmi.2018.08.009 . PMID   30145399.
  81. 1 2 Beans, Carolyn (2018-01-02). "News Feature: Can microbes keep time for forensic investigators?". Proceedings of the National Academy of Sciences. 115 (1): 3–6. doi: 10.1073/pnas.1718156114 . PMC   5776831 . PMID   29295964.
  82. "What are diatoms and what can they tell us about water quality?". APEM. Retrieved 2023-05-06.
  83. National Institute of Justice (March 2016). "Creating a Plan to Test a Large Number of Sexual Assault Kits" (PDF).