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Nature Genetics|January 29, 2015
Using iPSCs and genomics to catch CNVs in the actAlexander Eckehart Urban, Carolin Purmann
Research Square|May 20, 2024
Prioritizing disease-related rare variants by integrating gene expression dataHanmin Guo, Alexander Eckehart Urban, Wing Hung Wong
Biorxiv : the Preprint Server for Biology|April 2, 2024
Prioritizing disease-related rare variants by integrating gene expression dataHanmin Guo, Alexander Eckehart Urban, Wing Hung Wong
Plos Genetics|September 30, 2024
Prioritizing disease-related rare variants by integrating gene expression dataHanmin Guo, Alexander Eckehart Urban, Wing Hung Wong
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2012
Extensive genetic variation in somatic human tissuesMaeve O'Huallachain, Konrad J Karczewski, Sherman M Weissman, et al.
Genome Research|September 4, 2008
MEDME: an experimental and analytical methodology for the estimation of DNA methylation levels based on microarray derived MeDIP-enrichmentMattia Pelizzola, Yasuo Koga, Alexander Eckehart Urban, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2008
A procedure for highly specific, sensitive, and unbiased whole-genome amplificationXinghua Pan, Alexander Eckehart Urban, Dean Palejev, et al.
Scientific Reports|May 15, 2020
CNN-Peaks: ChIP-Seq peak detection pipeline using convolutional neural networks that imitate human visual inspectionDongpin Oh, J Seth Strattan, Junho K Hur, et al.
Current Opinion in Structural Biology|May 31, 2008
The current excitement about copy-number variation: how it relates to gene duplications and protein familiesJan O Korbel, Philip M Kim, Xueying Chen, et al.
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