Måns Magnusson

Bioinform. · 2014–2016

A researcher in the Science corpus: 2 papers; trusts 0 researchers and is trusted by 2 researchers here, as inferred from the citation graph.

Who trusts Måns Magnusson overall

  1. Guilherme de Sena Brandine

Papers from Måns Magnusson's perspective

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

  1. The Sequence Alignment/Map format and SAMtools (Bioinform.)
  2. An integrated map of genetic variation from 1,092 human genomes
  3. Natural genetic variation caused by small insertions and deletions in the human genome.
  4. A method and server for predicting damaging missense mutations
  5. A framework for variation discovery and genotyping using next-generation DNA sequencing data
  6. The Human Gene Mutation Database: 2008 update
  7. Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing (Genome Medicine)
  8. BFAST: An Alignment Tool for Large Scale Genome Resequencing (PLoS ONE)
  9. Critical assessment of methods of protein structure prediction (CASP): Round IV
  10. Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly (Bioinform.)

Their papers