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Accession: PRJNA380127 ID: 380127

The STR Sequencing Project (human)

The purpose of STRSeq is to facilitate the description of sequence-based alleles at the Short Tandem Repeat (STR) loci targeted in human identification assays. This collaborative effort of the international forensic DNA community, which has been endorsed by the executive board of the ISFG (International Society of Forensic Genetics), provides a framework for communication among laboratories. Each record contains: (a) observed sequence of an STR region, (b) annotation of the repeat region (“bracketing”) and flanking region polymorphisms, (c) information regarding the sequencing assay and data quality, and (d) backward compatible length-based allelic designation. Data within the umbrella project is organized into locus sub-projects, and can be accessed by browsing, BLAST searching, or ftp download at NCBI. For comments or questions, please contact strseq@nist.gov.
AccessionPRJNA380127
TypeUmbrella project
Publications (total 12)
  • Steffen CR et al., "A multi-dimensional evaluation of the 'NIST 1032' sample set across four forensic Y-STR multiplexes.", Forensic Sci Int Genet, 2022 Mar;57:102655
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SubmissionRegistration date: 22-Mar-2017
National Institute of Standards and Technology
Related Resources
RelevanceHuman Identification
Project Data:
Resource NameNumber
of Links
Sequence data
Nucleotide (Genomic DNA)2593
Publications
PubMed11
PMC5
The STR Sequencing Project (human) encompasses the following 4 sub-projects:
Project TypeNumber of Projects
Umbrella project4
BioProject
accession
NameTitle
PRJNA380345Homo sapiensSTRSeq Commonly Used Autosomal STR Loci (National Institute of Standards...)
PRJNA380346Homo sapiensSTRSeq Alternate Autosomal STR Loci (National Institute of Standards...)
PRJNA380347Homo sapiensSTRSeq Y-Chromosomal STR Loci (National Institute of Standards...)
PRJNA380348Homo sapiensSTRSeq X-Chromosomal STR Loci (National Institute of Standards...)

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