U.S. population data for human identification markers
Data and Resources
-
MS Excel FileXLS
Supplementary_Table3_MotifPatterns.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Supplementary_Table4_PopulationStatistics.xlsx
-
Text FileTEXT
-
Text FileTEXT
README_X-STR.txt
-
Text FileTEXT
-
Text FileTEXT
-
Text FileTEXT
-
MS Excel FileXLS
Supplemental_File_2.xlsx
-
Text FileTEXT
-
DOI Access for Sequence-based U.S. population...HTML
persistent identifier for Sequence-based U.S. population data for 27...
-
PDF FilePDF
Figure%20S1ab.pdf
-
Text FileTEXT
-
Text FileTEXT
README_Y-STR.txt
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S1.%20CE%20and%20Sanger%20primers.xlsx
-
PDF FilePDF
NIST1036_auSTR_Seq_SuppFile1.pdf
-
Text FileTEXT
-
MS Excel FileXLS
NIST1036_auSTR_Seq_SuppTables.xlsx
-
Text FileTEXT
-
Text FileTEXT
README_auSTR.txt
-
Text FileTEXT
-
Text FileTEXT
README_SE33.txt
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S10.%20Duplications%20and%20somatic%20mutants.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S11.%20Increase%20of%20allelic%20diversity%20by%20sequencing.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S12.%20Flanking%20region%20polymorphisms.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S13.%20DYS481%20nomenclature%20alternatives.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S2.%20Y-STR%20sequence%20ranges.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S3.%20Allele%20frequency%20table.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S4.%20Allele%20call%20table.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S5.%20Haplotype%20frequencies%20and%20haplotype-...
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S6.%20Allele-level%20forensic%20statistics.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S7.%20Haplotype%20pairs.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S8.%20AMOVA%20results.xlsx
-
Text FileTEXT
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S9.%20Locus%20mutation%20rates.xlsx
-
Text FileTEXT
-
Text FileTEXT
README_IISNP.txt
-
MS Word FileDOC
Supplemental%20Figures%20and%20Captions.docx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S1%20Allele%20Frequencies.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S2%20Forensic%20Parameters.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S3%20Linkage%20Disequilibrium.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S4%20Hardy-Weinberg%20Equilibrium.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S5%20Microhaplotype%20Frequencies.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S6%20Novel%20Microhaplotypes.xlsx
-
Text FileTEXT
-
PDF FilePDF
Figure%20S1ab.pdf
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S10.%20Duplications%20and%20somatic%20mutants.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S11.%20Increase%20of%20allelic%20diversity%20by%20sequencing.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S12.%20Flanking%20region%20polymorphisms.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S13.%20DYS481%20nomenclature%20alternatives.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S1.%20CE%20and%20Sanger%20primers.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S2.%20Y-STR%20sequence%20ranges.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S3.%20Allele%20frequency%20table.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S4.%20Allele%20call%20table.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S5.%20Haplotype%20frequencies%20and%20haplotype-...
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S6.%20Allele-level%20forensic%20statistics.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S7.%20Haplotype%20pairs.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S8.%20AMOVA%20results.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Table%20S9.%20Locus%20mutation%20rates.xlsx
-
Text FileTEXT
-
Text FileTEXT
-
MS Excel FileXLS
Supplementary_Table1_ExtendedFlank.xlsx
-
Text FileTEXT
-
MS Excel FileXLS
Supplementary_Table2_Frequency.xlsx
-
Text FileTEXT
| Field | Value |
|---|---|
| accessLevel | public |
| bureauCode | {006:55} |
| catalog_@context | https://project-open-data.cio.gov/v1.1/schema/data.json |
| catalog_conformsTo | https://project-open-data.cio.gov/v1.1/schema |
| catalog_describedBy | https://project-open-data.cio.gov/v1.1/schema/catalog.json |
| identifier | 6998B81EF78777B2E05324570681D4DC1911 |
| language | {en} |
| license | https://www.nist.gov/open/license |
| modified | 2023-04-19 00:00:00 |
| programCode | {006:045} |
| publisher | National Institute of Standards and Technology |
| references | {https://doi.org/10.1016/j.fsigen.2021.102655} |
| replaces | 6998B81EF78777B2E05324570681D4DC1911 |
| resource-type | Dataset |
| source_datajson_identifier | true |
| source_hash | 6ee17d5f3332d4ce8ec2152324d002ab5bb8bec4 |
| source_schema_version | 1.1 |
| theme | {"Forensics:DNA and biological evidence"} |
| Groups |
|
| Tags |
|
| isopen | False |
| license_id | other-license-specified |
| license_title | other-license-specified |
| maintainer | Katherine Gettings |
| maintainer_email | katherine.gettings@nist.gov |
| metadata_created | 2025-09-23T18:47:25.636231 |
| metadata_modified | 2025-09-23T18:47:25.636237 |
| notes | The primary data consist of allele or haplotype frequencies for N=1036 anonymized U.S. population samples. Additional files are supplements to the associated publications. Any changes to spreadsheets are listed in the "Change Log" tab within each spreadsheet. DOI numbers for associated publications are listed below, under "References". |
| num_resources | 97 |
| num_tags | 15 |
| title | U.S. population data for human identification markers |