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Author: Chunlin Xiao

  • Most recently observed institution: National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, 8600 Rockville Pike, Bethesda, MD 20894, USA

Rankings

  • All-time downloads: 57,072 (rank: 2,738 )
  • Categories:
    • bioinformatics: 3,242 (rank: 4,430 (tie) )
    • genomics: 53,830 (rank: 170 )

Downloads per author, site-wide

Preprints

A complete reference genome improves analysis of human genetic variation

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The complete sequence of a human genome

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  • Downloaded 33,007 times
  • Download rankings, all-time:
    • Site-wide: 217
    • In genomics: 10
  • Year to date:
    • Site-wide: 40
  • Since beginning of last month:
    • Site-wide: 8

Extensive sequencing of seven human genomes to characterize benchmark reference materials

genomics more details view paper
  • Downloaded 6,421 times
  • Download rankings, all-time:
    • Site-wide: 1,616
    • In genomics: 134
  • Year to date:
    • Site-wide: 40,002
  • Since beginning of last month:
    • Site-wide: 44,001

A robust benchmark for germline structural variant detection

genomics more details view paper
  • Downloaded 6,094 times
  • Download rankings, all-time:
    • Site-wide: 1,755
    • In genomics: 151
  • Year to date:
    • Site-wide: 5,528
  • Since beginning of last month:
    • Site-wide: 6,200

Reproducible integration of multiple sequencing datasets to form high-confidence SNP, indel, and reference calls for five human genome reference materials

genomics more details view paper
  • Downloaded 3,898 times
  • Download rankings, all-time:
    • Site-wide: 3,291
    • In genomics: 351
  • Year to date:
    • Site-wide: 20,913
  • Since beginning of last month:
    • Site-wide: 20,663

Establishing reference samples for detection of somatic mutations and germline variants with NGS technologies

bioinformatics more details view paper
  • Downloaded 2,841 times
  • Download rankings, all-time:
    • Site-wide: 5,124
    • In bioinformatics: 522
  • Year to date:
    • Site-wide: 8,265
  • Since beginning of last month:
    • Site-wide: 11,470

Benchmarking challenging small variants with linked and long reads

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  • Downloaded 2,040 times
  • Download rankings, all-time:
    • Site-wide: 8,268
    • In genomics: 864
  • Year to date:
    • Site-wide: 3,161
  • Since beginning of last month:
    • Site-wide: 3,144

SVCurator: A Crowdsourcing app to visualize evidence of structural variants for the human genome

genomics more details view paper
  • Downloaded 1,029 times
  • Download rankings, all-time:
    • Site-wide: 22,933
    • In genomics: 2,186
  • Year to date:
    • Site-wide: 64,977
  • Since beginning of last month:
    • Site-wide: 41,891

Towards a Comprehensive Variation Benchmark for Challenging Medically-Relevant Autosomal Genes

genomics more details view paper
  • Downloaded 906 times
  • Download rankings, all-time:
    • Site-wide: 27,504
    • In genomics: 2,512
  • Year to date:
    • Site-wide: 3,235
  • Since beginning of last month:
    • Site-wide: 447

High-coverage, long-read sequencing of Han Chinese trio reference samples.

genomics more details view paper
  • Downloaded 435 times
  • Download rankings, all-time:
    • Site-wide: 69,406
    • In genomics: 4,824
  • Year to date:
    • Site-wide: 136,855
  • Since beginning of last month:
    • Site-wide: 127,489

Personalized genome assembly for accurate cancer somatic mutation discovery using cancer-normal paired reference samples

bioinformatics more details view paper
  • Downloaded 401 times
  • Download rankings, all-time:
    • Site-wide: 75,076
    • In bioinformatics: 7,006
  • Year to date:
    • Site-wide: 10,626
  • Since beginning of last month:
    • Site-wide: 22,793

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