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Method

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly

  • Ilari Scheinin
  • Daoud Sie
  • Henrik Bengtsson
  • Mark A. van de Wiel
  • Adam B. Olshen
  • Hinke F. van Thuijl Hendrik F. van Essen Paul P. Eijk François Rustenburg Gerrit A. Meijer Jaap C. Reijneveld
  • ... [+6 authors] ...,
  • Pieter Wesseling
  • Daniel Pinkel
  • Donna G. Albertson
  • Bauke Ylstra
  • First Published September 18, 2014
Method

Combining RT-PCR-seq and RNA-seq to catalog all genic elements encoded in the human genome

  • Cédric Howald
  • Andrea Tanzer
  • Jacqueline Chrast
  • Felix Kokocinski
  • Thomas Derrien
  • Nathalie Walters Jose M. Gonzalez Adam Frankish Bronwen L. Aken Thibaut Hourlier Jan-Hinnerk Vogel Simon White Stephen Searle
  • ... [+8 authors] ...,
  • Jennifer Harrow
  • Tim J. Hubbard
  • Roderic Guigó
  • Alexandre Reymond
  • First Published September 5, 2012
Method

Estimation of alternative splicing variability in human populations

  • Mar Gonzàlez-Porta
  • Miquel Calvo
  • Michael Sammeth
  • Roderic Guigó
  • First Published November 23, 2011
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