Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,580 bioRxiv papers from 297,970 authors.

Downloads per author, site-wide

Preprints

Creating a universal SNP and small indel variant caller with deep neural networks

• Downloaded 35,218 times
• Download rankings, all-time:
  • Site-wide: 10 out of 67,466
  • In genomics: 3 out of 4,579
• Year to date:
  • Site-wide: 120 out of 67,466
• Since beginning of last month:
  • Site-wide: 545 out of 67,466

Analysis of protein-coding genetic variation in 60,706 humans

• Downloaded 21,535 times
• Download rankings, all-time:
  • Site-wide: 27 out of 67,466
  • In genomics: 7 out of 4,579
• Year to date:
  • Site-wide: 3,484 out of 67,466
• Since beginning of last month:
  • Site-wide: 9,883 out of 67,466

A deep learning approach to pattern recognition for short DNA sequences

• Downloaded 7,012 times
• Download rankings, all-time:
  • Site-wide: 242 out of 67,466
  • In bioinformatics: 39 out of 6,645
• Year to date:
  • Site-wide: 128 out of 67,466
• Since beginning of last month:
  • Site-wide: 905 out of 67,466

Scaling accurate genetic variant discovery to tens of thousands of samples

• Downloaded 4,437 times
• Download rankings, all-time:
  • Site-wide: 562 out of 67,466
  • In genomics: 148 out of 4,579
• Year to date:
  • Site-wide: 783 out of 67,466
• Since beginning of last month:
  • Site-wide: 1,003 out of 67,466

CrowdVariant: a crowdsourcing approach to classify copy number variants

• Downloaded 1,206 times
• Download rankings, all-time:
  • Site-wide: 5,734 out of 67,466
  • In genomics: 966 out of 4,579
• Year to date:
  • Site-wide: 39,563 out of 67,466
• Since beginning of last month:
  • Site-wide: 41,219 out of 67,466