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Nature genetics, ISSN 1061-4036, 11/2018, Volume 50, Issue 11, pp. 1615 - 1615
In the version of this article published, the P values for the enrichment of single mutation categories were inadvertently not corrected for multiple testing.... 
Mutation
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 2015, Volume 5, pp. 45 - 45
The identification of DNA copy numbers from short-read sequencing data remains a challenge for both technical and algorithmic reasons. The raw data for these... 
Signal processing | Whole-genome Sequencing | Clinical genomics | Structural variation | Depth of coverage | structural variation | clinical genomics | depth of coverage | Whole-genome sequencing
Journal Article
Human genome variation, ISSN 2054-345X, 2016, Volume 3, Issue 1, pp. 15060 - 15060
Currently, the best clinical predictor for inflammatory bowel disease (IBD) is family history. Over 163 sequence variants have been associated with IBD in... 
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2015, Volume 97, Issue 3, pp. 475 - 482
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2015, Volume 112, Issue 11, pp. 3576 - 3581
Journal Article
Journal Article
European Journal of Immunology, ISSN 0014-2980, 04/2015, Volume 45, Issue 4, pp. 1192 - 1205
Journal Article
Journal Article
Journal Article