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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 73,536 bioRxiv papers from 320,015 authors.

Author: Dale Muzzey

Rankings

  • All-time downloads: 6,855 (rank: 9,080 (tie) out of 320,022)
  • Categories:
    • genetics: 4,391 (rank: 3,319 out of 31,351)
    • genomics: 2,464 (rank: 6,374 (tie) out of 35,692)

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 1,353 times
  • Download rankings, all-time:
    • Site-wide: 5,282 out of 73,536
    • In genomics: 911 out of 4,879
  • Year to date:
    • Site-wide: 25,037 out of 73,536
  • Since beginning of last month:
    • Site-wide: 25,037 out of 73,536

Systematic Design and Comparison of Expanded Carrier Screening Panels

genetics more details view paper
  • Downloaded 1,345 times
  • Download rankings, all-time:
    • Site-wide: 5,335 out of 73,536
    • In genetics: 420 out of 4,034
  • Year to date:
    • Site-wide: 15,705 out of 73,536
  • Since beginning of last month:
    • Site-wide: 15,705 out of 73,536

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 1,223 times
  • Download rankings, all-time:
    • Site-wide: 6,254 out of 73,536
    • In genetics: 485 out of 4,034
  • Year to date:
    • Site-wide: 21,657 out of 73,536
  • Since beginning of last month:
    • Site-wide: 21,657 out of 73,536

Genetic influences on translation in yeast

genetics more details view paper
  • Downloaded 1,100 times
  • Download rankings, all-time:
    • Site-wide: 7,461 out of 73,536
    • In genetics: 580 out of 4,034
  • Year to date:
    • Site-wide: 57,081 out of 73,536
  • Since beginning of last month:
    • Site-wide: 57,080 out of 73,536

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 884 times
  • Download rankings, all-time:
    • Site-wide: 10,633 out of 73,536
    • In genomics: 1,556 out of 4,879
  • Year to date:
    • Site-wide: 15,229 out of 73,536
  • Since beginning of last month:
    • Site-wide: 15,229 out of 73,536

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

genetics more details view paper
  • Downloaded 497 times
  • Download rankings, all-time:
    • Site-wide: 24,212 out of 73,536
    • In genetics: 1,578 out of 4,034
  • Year to date:
    • Site-wide: 36,848 out of 73,536
  • Since beginning of last month:
    • Site-wide: 36,848 out of 73,536

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 227 times
  • Download rankings, all-time:
    • Site-wide: 50,638 out of 73,536
    • In genomics: 4,086 out of 4,879
  • Year to date:
    • Site-wide: 65,793 out of 73,536
  • Since beginning of last month:
    • Site-wide: 65,408 out of 73,536

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

genetics more details view paper
  • Downloaded 226 times
  • Download rankings, all-time:
    • Site-wide: 50,856 out of 73,536
    • In genetics: 3,012 out of 4,034
  • Year to date:
    • Site-wide: 50,768 out of 73,536
  • Since beginning of last month:
    • Site-wide: 50,769 out of 73,536

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