Skip to main content
U.S. flag

An official website of the United States government

This site is currently in beta, and your feedback is helping shape its ongoing development.

Return to search results

Sequence-based allelic variations and frequencies for 22 autosomal STR loci in the Lebanese population - Supplementary material

Published by National Institute of Standards and Technology | National Institute of Standards and Technology | Metadata Last Checked: August 02, 2025 | Last Modified: 2023-04-10 00:00:00
This data repository is meant to provide the supplementary files, tables, and figures included in the peer-reviewed research article entitled: "Sequence-based allelic variations and frequencies for 22 autosomal STR Loci in the Lebanese population". The article can be found at the following link (https://doi.org/10.1016/j.fsigen.2023.102872) and describes the sequencing of the 22 autosomal Short Tandem Repeat (aSTR) loci, using the PowerSeq 46GY System Prototype, in 195 individuals of self-reported Lebanese admixed ancestry. The supplemental files contain the sequence strings for each allele at each autosomal STR locus, length- and sequence- based allelic frequencies, quality control metrics for the sequencing runs, flanking region polymorphisms, as well as population and forensic genetic statistics. Any future changes to the supplements will be listed in the "Change Log" tab within each spreadsheet.

Resources

30 resources available

  • Supplementary File 1 - STRait Razor v3 Config

    APPLICATION/OCTET-STREAM
  • Supplementary File 2 - Sequence Ranges

    TEXT/PLAIN
  • Resource 3

    TEXT/PLAIN
  • MDS plot for Lebanese and four U.S. populations

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.PRESENTATIONML.PRESENTATION
  • Population tree for Lebanese and four U.S. populations

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.PRESENTATIONML.PRESENTATION
  • Lebanese population structure using unsupervised clustering

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.PRESENTATIONML.PRESENTATION
  • STRait Razor v3 configuration file for the 22 autosomal STRs identified by the PowerSeq 46GY assay

    APPLICATION/OCTET-STREAM
  • GRCh38 coordinate ranges used to adjust the sequences identified by both PowerSeq 46GY and ForenSeq Signature kits

    TEXT/PLAIN
  • Quality control metrics for the sequencing runs

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 1. Quality control metrics for the sequencing runs

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Linkage disequilibrium

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 10. Linkage disequilibrium

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • AMOVA test among and within the 5 studied populations

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Locus-by-locus FST and p-values

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Pairwise FST estimates and permutation test across five populations

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Average coverage of allelic sequences

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Average Hb across sequencing runs

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 3. Average Hb across sequencing runs

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Sequence-based allelic frequencies

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 4. Sequence-based allelic frequencies

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Allelic gains by sequencing

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 5. Allelic gains by sequencing

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Flanking region polymorphisms

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 6. Flanking region polymorphisms

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Length-based allelic frequencies

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 7. Length-based allelic frequencies

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Polymorphism Information Content, Power of discrimination, and Power of exclusion

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 8. Polymorphism Information Content, Power of discrimination, and Power of exclusion

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Match probability and Typical Paternity Index

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET
  • Supplementary Table 9. Match probability and Typical Paternity Index

    APPLICATION/VND.OPENXMLFORMATS-OFFICEDOCUMENT.SPREADSHEETML.SHEET

data.gov

An official website of the GSA's Technology Transformation Services

Looking for U.S. government information and services?
Visit USA.gov