Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,145 bioRxiv papers from 295,454 authors.

Downloads per author, site-wide

Preprints

Multiplexing droplet-based single cell RNA-sequencing using natural genetic barcodes

• Downloaded 4,591 times
• Download rankings, all-time:
  • Site-wide: 514 out of 67,174
  • In bioinformatics: 104 out of 6,627
• Year to date:
  • Site-wide: 8,937 out of 67,174
• Since beginning of last month:
  • Site-wide: 10,364 out of 67,174

A reference panel of 64,976 haplotypes for genotype imputation

• Downloaded 4,450 times
• Download rankings, all-time:
  • Site-wide: 554 out of 67,174
  • In genetics: 56 out of 3,777
• Year to date:
  • Site-wide: 42,197 out of 67,174
• Since beginning of last month:
  • Site-wide: 58,859 out of 67,174

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

• Downloaded 4,419 times
• Download rankings, all-time:
  • Site-wide: 562 out of 67,174
  • In genomics: 147 out of 4,566
• Year to date:
  • Site-wide: 2,022 out of 67,174
• Since beginning of last month:
  • Site-wide: 13,041 out of 67,174

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

• Downloaded 4,164 times
• Download rankings, all-time:
  • Site-wide: 634 out of 67,174
  • In genomics: 164 out of 4,566
• Year to date:
  • Site-wide: 128 out of 67,174
• Since beginning of last month:
  • Site-wide: 643 out of 67,174

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

• Downloaded 2,169 times
• Download rankings, all-time:
  • Site-wide: 2,115 out of 67,174
  • In bioinformatics: 431 out of 6,627
• Year to date:
  • Site-wide: 13,060 out of 67,174
• Since beginning of last month:
  • Site-wide: 27,123 out of 67,174

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

• Downloaded 1,775 times
• Download rankings, all-time:
  • Site-wide: 2,984 out of 67,174
  • In genomics: 588 out of 4,566
• Year to date:
  • Site-wide: 39,523 out of 67,174
• Since beginning of last month:
  • Site-wide: 24,569 out of 67,174

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

• Downloaded 1,438 times
• Download rankings, all-time:
  • Site-wide: 4,255 out of 67,174
  • In genetics: 360 out of 3,777
• Year to date:
  • Site-wide: 3,902 out of 67,174
• Since beginning of last month:
  • Site-wide: 13,865 out of 67,174

emeraLD: Rapid Linkage Disequilibrium Estimation with Massive Data Sets

• Downloaded 1,118 times
• Download rankings, all-time:
  • Site-wide: 6,468 out of 67,174
  • In bioinformatics: 1,200 out of 6,627
• Year to date:
  • Site-wide: 5,669 out of 67,174
• Since beginning of last month:
  • Site-wide: 17,525 out of 67,174

Narrow-sense heritability estimation of complex traits using identity-by-descent information.

• Downloaded 917 times
• Download rankings, all-time:
  • Site-wide: 8,897 out of 67,174
  • In genetics: 663 out of 3,777
• Year to date:
  • Site-wide: 17,232 out of 67,174
• Since beginning of last month:
  • Site-wide: 27,628 out of 67,174

Population-scale study of eRNA transcription reveals bipartite functional enhancer architecture

• Downloaded 685 times
• Download rankings, all-time:
  • Site-wide: 13,794 out of 67,174
  • In genomics: 1,855 out of 4,566
• Year to date:
  • Site-wide: 10,830 out of 67,174
• Since beginning of last month:
  • Site-wide: 14,775 out of 67,174

Imputation aware tag SNP selection to improve power for multi-ethnic association studies

• Downloaded 676 times
• Download rankings, all-time:
  • Site-wide: 14,057 out of 67,174
  • In genomics: 1,874 out of 4,566
• Year to date:
  • Site-wide: 52,828 out of 67,174
• Since beginning of last month:
  • Site-wide: 49,934 out of 67,174

Integrating Comprehensive Functional Annotations to Boost Power and Accuracy in Gene-Based Association Analysis

• Downloaded 460 times
• Download rankings, all-time:
  • Site-wide: 23,370 out of 67,174
  • In genetics: 1,552 out of 3,777
• Year to date:
  • Site-wide: 7,386 out of 67,174
• Since beginning of last month:
  • Site-wide: 9,151 out of 67,174

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

• Downloaded 459 times
• Download rankings, all-time:
  • Site-wide: 23,397 out of 67,174
  • In genomics: 2,561 out of 4,566
• Year to date:
  • Site-wide: 7,405 out of 67,174
• Since beginning of last month:
  • Site-wide: 16,922 out of 67,174

Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis

• Downloaded 313 times
• Download rankings, all-time:
  • Site-wide: 34,912 out of 67,174
  • In genomics: 3,274 out of 4,566
• Year to date:
  • Site-wide: 33,706 out of 67,174
• Since beginning of last month:
  • Site-wide: 50,635 out of 67,174

Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability

• Downloaded 294 times
• Download rankings, all-time:
  • Site-wide: 36,867 out of 67,174
  • In genetics: 2,283 out of 3,777
• Year to date:
  • Site-wide: 63,541 out of 67,174
• Since beginning of last month:
  • Site-wide: 47,516 out of 67,174

Heterogeneous transcriptome response to DNA damage at single cell resolution.

• Downloaded 244 times
• Download rankings, all-time:
  • Site-wide: 42,595 out of 67,174
  • In cell biology: 2,075 out of 3,257
• Year to date:
  • Site-wide: 19,692 out of 67,174
• Since beginning of last month:
  • Site-wide: 14,577 out of 67,174