M. Eberle

bioRxiv · 2004–2019

A researcher in the Science corpus: 7 papers; trusts 0 researchers and is trusted by 4 researchers here, as inferred from the citation graph.

Whom M. Eberle trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. Gonçalo R. Abecasis
  2. Matthew Stephens

Who trusts M. Eberle overall

  1. Daniel C. Koboldt
  2. Reedik Mägi
  3. Jonathan Marchini
  4. David J. Balding
  5. Arang Rhie
  6. Ben Langmead
  7. Sharon R. Browning
  8. Frank Steemers

Papers from M. Eberle's perspective

Ordered by how strongly the researchers M. Eberle trusts endorse each paper. Same corpus, a different order for every researcher.

  1. Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
  2. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)
  3. The Sequence Alignment/Map format and SAMtools (Bioinform.)
  4. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
  5. Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
  6. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
  7. Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs (Bioinform.)
  8. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 (Science)
  9. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease (Nature Genetics)
  10. De novo assembly and genotyping of variants using colored de Bruijn graphs (Nature Genetics)

Their papers