Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,198 bioRxiv papers from 276,129 authors.

Downloads per author, site-wide

Preprints

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

• Downloaded 34,679 times
• Download rankings, all-time:
  • Site-wide: 10 out of 62,198
  • In genomics: 3 out of 4,277
• Year to date:
  • Site-wide: 111 out of 62,198
• Since beginning of last month:
  • Site-wide: 278 out of 62,198

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

• Downloaded 21,430 times
• Download rankings, all-time:
  • Site-wide: 24 out of 62,198
  • In genomics: 6 out of 4,277
• Year to date:
  • Site-wide: 3,218 out of 62,198
• Since beginning of last month:
  • Site-wide: 3,463 out of 62,198

A deep learning approach to pattern recognition for short DNA sequences

• Downloaded 6,633 times
• Download rankings, all-time:
  • Site-wide: 244 out of 62,198
  • In bioinformatics: 41 out of 6,209
• Year to date:
  • Site-wide: 109 out of 62,198
• Since beginning of last month:
  • Site-wide: 300 out of 62,198

Scaling accurate genetic variant discovery to tens of thousands of samples

• Downloaded 3,984 times
• Download rankings, all-time:
  • Site-wide: 629 out of 62,198
  • In genomics: 166 out of 4,277
• Year to date:
  • Site-wide: 1,000 out of 62,198
• Since beginning of last month:
  • Site-wide: None out of 62,198

CrowdVariant: a crowdsourcing approach to classify copy number variants

• Downloaded 1,185 times
• Download rankings, all-time:
  • Site-wide: 5,247 out of 62,198
  • In genomics: 902 out of 4,277
• Year to date:
  • Site-wide: 35,140 out of 62,198
• Since beginning of last month:
  • Site-wide: 30,599 out of 62,198