Author: Ryan Poplin

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Preprints

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

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  • In genomics: 4 out of 5,828
• Year to date:
  • Site-wide: 952 out of 92,411
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  • Site-wide: 1,521 out of 92,411

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

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  • Site-wide: 70 out of 92,411
  • In genomics: 10 out of 5,828
• Year to date:
  • Site-wide: 17,428 out of 92,411
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  • Site-wide: 17,849 out of 92,411

A deep learning approach to pattern recognition for short DNA sequences

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  • Site-wide: 325 out of 92,411
  • In bioinformatics: 40 out of 8,662
• Year to date:
  • Site-wide: 1,180 out of 92,411
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  • Site-wide: 3,853 out of 92,411

Scaling accurate genetic variant discovery to tens of thousands of samples

• Downloaded 6,137 times
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  • Site-wide: 551 out of 92,411
  • In genomics: 116 out of 5,828
• Year to date:
  • Site-wide: 862 out of 92,411
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  • Site-wide: 935 out of 92,411

CrowdVariant: a crowdsourcing approach to classify copy number variants

• Downloaded 1,276 times
• Download rankings, all-time:
  • Site-wide: 7,985 out of 92,411
  • In genomics: 1,214 out of 5,828
• Year to date:
  • Site-wide: 66,774 out of 92,411
• Since beginning of last month:
  • Site-wide: 64,279 out of 92,411