Halacha meets DNA fingerprinting
Description
Scientific article
Abstract
The genetic code is stored within the sequences of
nitrogenous bases (i.e., adenine, thymine, cytosine, and
guanine) on DNA of nuclear chromosomes and on
mitochondrial DNA. Except for isolated mutations, an individual’s
DNA remains constant throughout life and forms that person’s
unique genetic code, controlling biochemical reactions, growth,
and development. About 99.9% of the human DNA sequences
are similar in every person, with only a very small amount of DNA
differing from individual to individual. These relatively minor
differences serve as genetic markers and are of sufficient quantity
to allow forensic scientists to distinguish one person from another
person. Genetic markers, the DNA sequences used to identify
(i.e., to mark) a specific location on a chromosome, include single
nucleotide polymorphisms (SNPs) and copy number variants
(CNVs). A SNP is a single base pair that differs among individuals.
For a SNP to be a genetic marker it must be present in at least
1% of the population, thereby excluding those genetic variants
that are too rare for general usefulness in genetic analyses. There
are millions of SNPs in the human genome. Consecutive SNPs
on the same DNA sequence of a chromosome are correlated, as
each arose in history as a single point mutation which then was
transmitted, surrounded by earlier SNPs, to descendants. Such a
cluster of SNPs, when located near enough to each other on a
chromosome, are transmitted as a unit (or, a haplotype). CNVs are
tandemly repeated DNA sequences, present in different numbers
of copies in different individuals. CNVs can range in size from
one a kilobase, a thousand base pairs, to a megabase, a million base
pairs. CNVs vary in number from person to person. A genetic
marker is identified by a probe, usually a short fragment of DNA
that is a few or a few dozen nucleotides in length. Both the genetic
marker and the probe are made single-stranded, with the genetic
marker detected by pairing (termed, hybridization) between the
complementar
Permanent Link(s)
https://hdl.handle.net/20.500.12202/8920Citation
Babich, H. (2014-2015). Halacha meets DNA fingerprinting. Derech HaTeva, 19, 55-59.
*This is constructed from limited available data and may be imprecise.
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