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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 59,974 bioRxiv papers from 266,630 authors.

Author: Dale Muzzey

Rankings

  • All-time downloads: 6,322 (rank: 7,694 (tie) out of 266,630)
  • Categories:
    • genetics: 4,079 (rank: 3,134 out of 27,028)
    • genomics: 2,243 (rank: 5,907 out of 31,184)

Downloads per author, site-wide

Preprints

Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole- Genome Sequencing and Single-Nucleotide Polymorphism Methods

genomics more details view paper
  • Downloaded 1,272 times
  • Download rankings, all-time:
    • Site-wide: 4,560 out of 59,974
    • In genomics: 816 out of 4,168
  • Year to date:
    • Site-wide: 11,298 out of 59,974
  • Since beginning of last month:
    • Site-wide: 29,501 out of 59,974

Systematic Design and Comparison of Expanded Carrier Screening Panels

genetics more details view paper
  • Downloaded 1,255 times
  • Download rankings, all-time:
    • Site-wide: 4,652 out of 59,974
    • In genetics: 384 out of 3,425
  • Year to date:
    • Site-wide: 38,306 out of 59,974
  • Since beginning of last month:
    • Site-wide: 29,876 out of 59,974

Development and validation of an expanded carrier screen that optimizes sensitivity via full-exon sequencing and panel-wide copy-number-variant identification

genetics more details view paper
  • Downloaded 1,158 times
  • Download rankings, all-time:
    • Site-wide: 5,320 out of 59,974
    • In genetics: 432 out of 3,425
  • Year to date:
    • Site-wide: 29,957 out of 59,974
  • Since beginning of last month:
    • Site-wide: 46,142 out of 59,974

Genetic influences on translation in yeast

genetics more details view paper
  • Downloaded 1,059 times
  • Download rankings, all-time:
    • Site-wide: 6,198 out of 59,974
    • In genetics: 508 out of 3,425
  • Year to date:
    • Site-wide: 57,952 out of 59,974
  • Since beginning of last month:
    • Site-wide: 54,454 out of 59,974

Software-assisted manual review of clinical NGS data: an alternative to routine Sanger sequencing confirmation with equivalent results in >15,000 hereditary cancer screens

genomics more details view paper
  • Downloaded 782 times
  • Download rankings, all-time:
    • Site-wide: 9,964 out of 59,974
    • In genomics: 1,465 out of 4,168
  • Year to date:
    • Site-wide: 7,742 out of 59,974
  • Since beginning of last month:
    • Site-wide: 21,394 out of 59,974

Clinical Impact and Cost-Effectiveness of a 176-Condition Expanded Carrier Screen

genetics more details view paper
  • Downloaded 434 times
  • Download rankings, all-time:
    • Site-wide: 21,705 out of 59,974
    • In genetics: 1,445 out of 3,425
  • Year to date:
    • Site-wide: 17,477 out of 59,974
  • Since beginning of last month:
    • Site-wide: 40,765 out of 59,974

Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene

genomics more details view paper
  • Downloaded 189 times
  • Download rankings, all-time:
    • Site-wide: 43,472 out of 59,974
    • In genomics: 3,575 out of 4,168
  • Year to date:
    • Site-wide: 42,850 out of 59,974
  • Since beginning of last month:
    • Site-wide: 45,805 out of 59,974

A Data-Driven Evaluation of the Size and Content of Expanded Carrier Screening Panels

genetics more details view paper
  • Downloaded 173 times
  • Download rankings, all-time:
    • Site-wide: 45,469 out of 59,974
    • In genetics: 2,743 out of 3,425
  • Year to date:
    • Site-wide: 36,328 out of 59,974
  • Since beginning of last month:
    • Site-wide: 36,679 out of 59,974

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