Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 70,230 bioRxiv papers from 306,630 authors.

Downloads per author, site-wide

Preprints

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

• Downloaded 35,531 times
• Download rankings, all-time:
  • Site-wide: 10 out of 70,230
  • In genomics: 3 out of 4,700
• Year to date:
  • Site-wide: 430 out of 70,230
• Since beginning of last month:
  • Site-wide: 424 out of 70,230

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

• Downloaded 21,567 times
• Download rankings, all-time:
  • Site-wide: 30 out of 70,230
  • In genomics: 7 out of 4,700
• Year to date:
  • Site-wide: 21,477 out of 70,230
• Since beginning of last month:
  • Site-wide: 18,446 out of 70,230

A deep learning approach to pattern recognition for short DNA sequences

• Downloaded 7,261 times
• Download rankings, all-time:
  • Site-wide: 237 out of 70,230
  • In bioinformatics: 38 out of 6,887
• Year to date:
  • Site-wide: 419 out of 70,230
• Since beginning of last month:
  • Site-wide: 848 out of 70,230

Scaling accurate genetic variant discovery to tens of thousands of samples

• Downloaded 4,550 times
• Download rankings, all-time:
  • Site-wide: 552 out of 70,230
  • In genomics: 144 out of 4,700
• Year to date:
  • Site-wide: 4,684 out of 70,230
• Since beginning of last month:
  • Site-wide: 1,352 out of 70,230

CrowdVariant: a crowdsourcing approach to classify copy number variants

• Downloaded 1,214 times
• Download rankings, all-time:
  • Site-wide: 5,932 out of 70,230
  • In genomics: 985 out of 4,700
• Year to date:
  • Site-wide: 34,623 out of 70,230
• Since beginning of last month:
  • Site-wide: 63,664 out of 70,230