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    <loc>/announcements/updated-alignment-file-2009-10-06/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/announcements/bam-statistics-files-added-ftp-site-2009-10-02/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/announcements/availability-qc-passed-fastq-files-2009-10-02/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/announcements/consensus-indel-call-sets-2009-05-15/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/announcements/initial-release-low-coverage-pilot-data-2009-02-15/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/announcements/first-data-release-snp-data-downloads-and-genome-browser-representing-four-high-covera/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/about-alignment-files-bam-and-cram/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/about-fastq-sequence-read-files/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/about-index-files/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/about-variant-identifiers/</loc>
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  </url>
  <url>
    <loc>/faq/about-vcf-variant-files/</loc>
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  </url>
  <url>
    <loc>/faq/are-the-igsr-variants-available-in-dbsnp/</loc>
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  <url>
    <loc>/faq/are-the-igsr-variants-available-in-genome-browsers/</loc>
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  </url>
  <url>
    <loc>/faq/are-the-variant-calls-in-igsr-phased/</loc>
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  </url>
  <url>
    <loc>/faq/are-there-any-genomic-regions-that-have-not-been-studied/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/are-there-any-statistics-about-how-much-sequence-data-is-in-igsr/</loc>
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  </url>
  <url>
    <loc>/faq/can-i-blast-against-the-sequences-in-igsr/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/can-i-convert-vcf-files-to-plinkped-format/</loc>
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  </url>
  <url>
    <loc>/faq/can-i-get-cell-lines-for-igsr-samples/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/can-i-get-phased-genotypes-and-haplotypes-for-the-individual-genomes/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/can-i-get-phenotype-gender-and-family-relationship-information-for-the-individuals/</loc>
    <lastmod></lastmod>
  </url>
  <url>
    <loc>/faq/can-i-map-your-variant-coordinates-between-different-genome-assemblies/</loc>
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  </url>
  <url>
    <loc>/faq/can-i-query-igsr-programmatically/</loc>
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  </url>
  <url>
    <loc>/faq/can-i-search-the-website/</loc>
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  </url>
  <url>
    <loc>/faq/can-i-use-the-igsr-data-for-imputation/</loc>
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  <url>
    <loc>/faq/can-i-volunteer-be-part-1000-genomes-project/</loc>
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  <url>
    <loc>/faq/do-i-need-a-password-to-access-igsr-data/</loc>
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  <url>
    <loc>/faq/do-i-need-permission-to-use-igsr-data-in-my-own-scientific-research/</loc>
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  </url>
  <url>
    <loc>/faq/do-you-have-any-ancient-or-prehistoric-genomes/</loc>
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  </url>
  <url>
    <loc>/faq/do-you-have-any-job-vacancies/</loc>
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  </url>
  <url>
    <loc>/faq/do-you-have-assembled-fasta-sequences-for-samples/</loc>
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  <url>
    <loc>/faq/do-you-have-structural-variation-data/</loc>
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  <url>
    <loc>/faq/does-the-1000-genomes-project-use-hapmap-data/</loc>
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  <url>
    <loc>/faq/have-you-calculated-linkage-disequilibrium-from-these-variants/</loc>
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  </url>
  <url>
    <loc>/faq/help-me-to-interpret-or-understand-more-about-a-genetic-disease-diagnosis/</loc>
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  </url>
  <url>
    <loc>/faq/help-me-to-interpret-or-understand-more-about-my-personal-genomics-data/</loc>
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  </url>
  <url>
    <loc>/faq/how-are-allele-frequencies-calculated/</loc>
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  </url>
  <url>
    <loc>/faq/how-can-i-get-all-variants-in-a-particular-gene/</loc>
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  </url>
  <url>
    <loc>/faq/how-can-i-get-gene-sequences-for-individuals/</loc>
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  </url>
  <url>
    <loc>/faq/how-can-i-get-vcfs-of-a-single-population-or-individual/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-I-cite-IGSR/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-contact-one-of-the-individuals-whose-genome-you-have-sampled/</loc>
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  <url>
    <loc>/faq/how-do-i-contact-you/</loc>
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  <url>
    <loc>/faq/how-do-i-find-out-about-new-releases/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-find-out-information-about-a-single-variant/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-find-specific-alignment-files/</loc>
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  <url>
    <loc>/faq/how-do-i-find-specific-sequence-read-files/</loc>
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  <url>
    <loc>/faq/how-do-i-find-specific-variant-files/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-find-the-familial-relationships-between-the-individuals/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-find-the-most-up-to-date-data/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-find-the-reference-genomes-files/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-get-a-genomic-region-sub-section-of-your-files/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-i-navigate-the-ftp-site-to-find-the-files-i-need/</loc>
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  </url>
  <url>
    <loc>/faq/how-do-you-calculate-ancestral-alleles/</loc>
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  </url>
  <url>
    <loc>/faq/how-many-individuals-have-been-sequenced-in-igsr-projects-and-how-were-they-selected/</loc>
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  <url>
    <loc>/faq/how-was-exome-and-exon-targetted-sequencing-used/</loc>
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  </url>
  <url>
    <loc>/faq/how-was-imputation-used-in-1000-genomes-to-fill-in-gaps-in-sequencing/</loc>
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    <loc>/faq/how-were-the-populations-defined/</loc>
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    <loc>/faq/is-the-sequencing-data-in-igsr-contaminated-with-mycoplasma/</loc>
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  </url>
  <url>
    <loc>/faq/is-there-any-fee-associated-with-using-andor-reproducing-the-data/</loc>
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  <url>
    <loc>/faq/is-there-gene-expression-andor-functional-annotation-available-for-the-samples/</loc>
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  </url>
  <url>
    <loc>/faq/there-is-a-corrupt-file-on-your-ftp-site/</loc>
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  <url>
    <loc>/faq/was-hla-diversity-studied-in-igsr/</loc>
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  <url>
    <loc>/faq/were-the-same-analysis-tools-used-for-every-sample-in-one-data-collection/</loc>
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  </url>
  <url>
    <loc>/faq/what-are-the-different-data-collections-available-for-1000-genomes/</loc>
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  </url>
  <url>
    <loc>/faq/what-are-your-filename-conventions/</loc>
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    <loc>/faq/what-do-the-population-codes-mean/</loc>
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    <loc>/faq/what-is-the-coverage-depth/</loc>
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  </url>
  <url>
    <loc>/faq/what-methods-were-used-for-generating-alignments/</loc>
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  <url>
    <loc>/faq/what-sequencing-platforms-and-methods-were-used-by-different-projects-within-igsr/</loc>
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  <url>
    <loc>/faq/what-tools-can-i-use-to-download-igsr-data/</loc>
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  <url>
    <loc>/faq/what-types-of-genotyping-data-do-you-have/</loc>
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  </url>
  <url>
    <loc>/faq/what-was-the-source-of-the-dna-for-sequencing/</loc>
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  <url>
    <loc>/faq/where-can-i-find-a-list-of-the-sequencing-and-analysis-done-for-each-individual/</loc>
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  <url>
    <loc>/faq/where-can-i-get-consequence-annotations-for-the-igsr-variants/</loc>
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  <url>
    <loc>/faq/where-were-the-sampling-locations/</loc>
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    <loc>/faq/which-datasets-include-related-individuals/</loc>
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    <loc>/faq/which-populations-are-part-of-your-study/</loc>
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    <loc>/faq/which-reference-assembly-do-you-use/</loc>
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  </url>
  <url>
    <loc>/faq/why-are-the-coordinates-of-some-variants-different-to-what-is-displayed-in-other-databases/</loc>
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  </url>
  <url>
    <loc>/faq/why-are-there-chr-11-and-chr-20-alignment-files-and-not-for-other-chromosomes/</loc>
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  </url>
  <url>
    <loc>/faq/why-are-there-differences-between-the-different-analyses-of-the-1000-genomes-samples/</loc>
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  </url>
  <url>
    <loc>/faq/why-are-there-duplicate-calls-in-the-phase-3-call-set/</loc>
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  <url>
    <loc>/faq/why-are-there-gaps-in-the-x-and-y-chromosome/</loc>
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    <loc>/faq/why-cant-i-find-one-of-your-variants-in-another-database/</loc>
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  <url>
    <loc>/faq/why-do-some-of-your-vcf-genotype-files-have-genotypes-of--in-them/</loc>
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    <loc>/faq/why-do-some-variants-in-the-phase1-release-have-an-zero-allele-frequency/</loc>
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    <loc>/faq/why-does-a-tabix-fetch-fail/</loc>
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    <loc>/faq/why-is-the-allele-frequency-different-from-allele-countallele-number/</loc>
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    <loc>/1000-genomes-annoucement-mailing-list/</loc>
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    <loc>/1000-genomes-browsers/</loc>
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    <loc>/1000-genomes-command-line-exercises-code-requirements/</loc>
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    <loc>/1000-genomes-project-publications/</loc>
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    <loc>/1000-genomes-summary/</loc>
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    <loc>/data-portal/data-collections/1000genomes/</loc>
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    <loc>/data-portal/data-collections/1000genomes_30x/</loc>
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    <loc>/data-portal/data-collections/1kg_ont_vienna/</loc>
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    <loc>/data-portal/data-collections/HGDP/</loc>
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  <url>
    <loc>/data-portal/data-collections/HGDP_transcriptome/</loc>
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  <url>
    <loc>/IGSR_disclaimer/</loc>
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  <url>
    <loc>/data_collections/gambian-genome-variation-project/README_gambian_genome_variation_project_datareuse_statement/</loc>
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  <url>
    <loc>/data_collections/hgsv_sv_discovery/README_hgsvc_datareuse_statement/</loc>
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    <loc>/data-portal/data-collections/SGDP/</loc>
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  <url>
    <loc>/about/</loc>
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  </url>
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    <loc>/allele-frequency-calculator-documentation/</loc>
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  <url>
    <loc>/analysis/</loc>
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    <loc>/ashg-2012-1000-genomes-tutorial-wednesday-7th-november-7-930pm/</loc>
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    <loc>/ashg-2012-poster/</loc>
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    <loc>/ashg-2014-1000-genomes-tutorial-sunday-october-19-8-930-pm-convention-center-room-24abc-upper-level/</loc>
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    <loc>/ashg13-1000-genomes-project-tutorial-october-23rd-boston-convention-exhibition-center-meetings-rooms/</loc>
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    <loc>/wiki/Analysis/Variant Call Format/VCF (Variant Call Format) version 4.0/encoding-structural-variants/</loc>
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    <loc>/forge-gwas-catalog-example-gallery11/</loc>
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    <loc>/wiki/Analysis/Variant Call Format/vcf-variant-call-format-version-40/</loc>
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    <loc>/wiki/Analysis/Variant Call Format/vcf-variant-call-format-version-41/</loc>
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    <loc>/wiki/Analysis/vcf4.0/</loc>
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  </urlset>
