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  2. List of Y-STR markers - Wikipedia

    en.wikipedia.org/wiki/List_of_Y-STR_markers

    The Y-STR markers in the following list are commonly used in forensic [1] and genealogical DNA testing. DYS454 is the least diverse, and multi-copy marker DYS464 is the most diverse Y-STR marker. The location on the Y-chromosome of numbered Y-STR markers can be roughly given with cytogenetic localization. For example, DYS449 is located at Yp11 ...

  3. De novo peptide sequencing - Wikipedia

    en.wikipedia.org/wiki/De_novo_peptide_sequencing

    For example, mass differences between a n and a n-1, b n and b n-1, c n and c n-1 are the same. Identify y n-1-ion at the high-mass end of the spectrum. Then continue to identify y n-2, y n-3... ions by matching mass differences with the amino acid residue masses (see Table 1). Look for the corresponding b-ions of the identified y-ions.

  4. Forensic DNA analysis - Wikipedia

    en.wikipedia.org/wiki/Forensic_DNA_analysis

    STR analysis can also be restricted to just the Y chromosome. Y-STR analysis can be used in cases that involve paternity or in familial searching as the Y chromosome is identical down the paternal line (except in cases where a mutation occurred). Certain multiplexing kits combine both autosomal and Y-STR loci into one kit further reducing the ...

  5. Sanger sequencing - Wikipedia

    en.wikipedia.org/wiki/Sanger_sequencing

    Common challenges of DNA sequencing with the Sanger method include poor quality in the first 15–40 bases of the sequence due to primer binding and deteriorating quality of sequencing traces after 700–900 bases. Base calling software such as Phred typically provides an estimate of quality to aid in trimming of low-quality regions of sequences.

  6. 2 base encoding - Wikipedia

    en.wikipedia.org/wiki/2_Base_Encoding

    These technologies generate hundreds of thousands of small sequence reads at one time. Well-known examples of such DNA sequencing methods include 454 pyrosequencing (introduced in 2005), the Solexa system (introduced in 2006) and the SOLiD system (introduced in 2007). These methods have reduced the cost from $0.01/base in 2004 to nearly $0.0001 ...

  7. DNA read errors - Wikipedia

    en.wikipedia.org/wiki/DNA_read_errors

    The most common sequencing method is the shotgun method, which is the method most probably used on sequence 2. Once a method is decided on, you have to specify the length of the bp reads you would like it to return. In the case of sequence 2, it returned 7-bp reads with all errors made during the process noted in red. [4]

  8. List of unsolved problems in biology - Wikipedia

    en.wikipedia.org/wiki/List_of_unsolved_problems...

    Unsolved problems relating to the structure and function of non-human organs, processes and biomolecules include: Korarchaeota (archaea). The metabolic processes of this phylum of archaea are so far unclear. Glycogen body. The function of this structure in the spinal cord of birds is not known. Arthropod head problem. A long-standing zoological ...

  9. Conversion table for Y chromosome haplogroups - Wikipedia

    en.wikipedia.org/wiki/Conversion_table_for_Y...

    The Y-Chromosome Consortium for many years left individual groups to maintain this standard. In 2008, they again published a comprehensive review of tree changes and retested samples. With this work, they strengthened their recommendation to move to a nomenclature system they referred to as shorthand ( Karafet 2008 ).