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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 73,582 bioRxiv papers from 320,155 authors.

Author: Ryan M. Layer

Rankings

  • All-time downloads: 19,864 (rank: 1,627 out of 319,996)
  • Categories:
    • bioinformatics: 8,968 (rank: 443 out of 27,758)
    • genomics: 10,896 (rank: 1,051 out of 35,691)

Downloads per author, site-wide

Preprints

SpeedSeq: Ultra-fast personal genome analysis and interpretation

bioinformatics more details view paper
  • Downloaded 5,138 times
  • Download rankings, all-time:
    • Site-wide: 476 out of 73,530
    • In bioinformatics: 93 out of 7,162
  • Year to date:
    • Site-wide: 19,269 out of 73,530
  • Since beginning of last month:
    • Site-wide: 19,269 out of 73,530

Efficient genotype compression and analysis of large genetic variation datasets

genomics more details view paper
  • Downloaded 3,173 times
  • Download rankings, all-time:
    • Site-wide: 1,195 out of 73,530
    • In genomics: 274 out of 4,879
  • Year to date:
    • Site-wide: 36,278 out of 73,530
  • Since beginning of last month:
    • Site-wide: 36,278 out of 73,530

A map of constrained coding regions in the human genome.

genomics more details view paper
  • Downloaded 2,912 times
  • Download rankings, all-time:
    • Site-wide: 1,396 out of 73,530
    • In genomics: 312 out of 4,879
  • Year to date:
    • Site-wide: 23,658 out of 73,530
  • Since beginning of last month:
    • Site-wide: 23,658 out of 73,530

Mapping and characterization of structural variation in 17,795 deeply sequenced human genomes

genomics more details view paper
  • Downloaded 2,450 times
  • Download rankings, all-time:
    • Site-wide: 1,906 out of 73,530
    • In genomics: 410 out of 4,879
  • Year to date:
    • Site-wide: 3,084 out of 73,530
  • Since beginning of last month:
    • Site-wide: 3,084 out of 73,530

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

genomics more details view paper
  • Downloaded 2,361 times
  • Download rankings, all-time:
    • Site-wide: 2,038 out of 73,530
    • In genomics: 429 out of 4,879
  • Year to date:
    • Site-wide: 56,011 out of 73,530
  • Since beginning of last month:
    • Site-wide: 56,011 out of 73,530

GIGGLE: a search engine for large-scale integrated genome analysis

bioinformatics more details view paper
  • Downloaded 1,464 times
  • Download rankings, all-time:
    • Site-wide: 4,630 out of 73,530
    • In bioinformatics: 889 out of 7,162
  • Year to date:
    • Site-wide: 61,581 out of 73,530
  • Since beginning of last month:
    • Site-wide: 61,581 out of 73,530

Vcfanno: fast, flexible annotation of genetic variants

bioinformatics more details view paper
  • Downloaded 1,162 times
  • Download rankings, all-time:
    • Site-wide: 6,803 out of 73,530
    • In bioinformatics: 1,243 out of 7,162
  • Year to date:
    • Site-wide: 39,551 out of 73,530
  • Since beginning of last month:
    • Site-wide: 39,551 out of 73,530

svtools: population-scale analysis of structural variation

bioinformatics more details view paper
  • Downloaded 730 times
  • Download rankings, all-time:
    • Site-wide: 14,195 out of 73,530
    • In bioinformatics: 2,269 out of 7,162
  • Year to date:
    • Site-wide: 38,727 out of 73,530
  • Since beginning of last month:
    • Site-wide: 38,727 out of 73,530

SV-plaudit: A cloud-based framework for manually curating thousands of structural variants

bioinformatics more details view paper
  • Downloaded 474 times
  • Download rankings, all-time:
    • Site-wide: 25,628 out of 73,530
    • In bioinformatics: 3,524 out of 7,162
  • Year to date:
    • Site-wide: 42,501 out of 73,530
  • Since beginning of last month:
    • Site-wide: 42,501 out of 73,530

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