Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nathan R Mattson"'
Autor:
Jacob R Heldenbrand, Saurabh Baheti, Matthew A Bockol, Travis M Drucker, Steven N Hart, Matthew E Hudson, Ravishankar K Iyer, Michael T Kalmbach, Katherine I Kendig, Eric W Klee, Nathan R Mattson, Eric D Wieben, Mathieu Wiepert, Derek E Wildman, Liudmila S Mainzer
Publikováno v:
BMC Bioinformatics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Use of the Genome Analysis Toolkit (GATK) continues to be the standard practice in genomic variant calling in both research and the clinic. Recently the toolkit has been rapidly evolving. Significant computational performance impr
Externí odkaz:
https://doaj.org/article/d1ba367575504c22a9097a3dd969475e
Autor:
Jacob R. Heldenbrand, Saurabh Baheti, Matthew A. Bockol, Travis M. Drucker, Steven N. Hart, Matthew E. Hudson, Ravishankar K. Iyer, Michael T. Kalmbach, Katherine I. Kendig, Eric W. Klee, Nathan R. Mattson, Eric D. Wieben, Mathieu Wiepert, Derek E. Wildman, Liudmila S. Mainzer
Publikováno v:
BMC Bioinformatics, Vol 20, Iss 1, Pp 1-2 (2019)
Following publication of the original article [1], the author explained that Table 2 is displayed incorrectly. The correct Table 2 is given below. The original article has been corrected.
Externí odkaz:
https://doaj.org/article/1d2bd5275f844ba98289f769d1c30948
Autor:
Michael T Kalmbach, Matthew E. Hudson, Derek E. Wildman, Eric D. Wieben, Liudmila Sergeevna Mainzer, Travis M. Drucker, Saurabh Baheti, Steven N. Hart, Eric W. Klee, Mathieu Wiepert, Ravishankar K. Iyer, Nathan R Mattson, Matthew A. Bockol, Jacob R Heldenbrand, Katherine I Kendig
Publikováno v:
BMC Bioinformatics, Vol 20, Iss 1, Pp 1-2 (2019)
Following publication of the original article [1], the author explained that Table 2 is displayed incorrectly. The correct Table 2 is given below. The original article has been corrected.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed17efc114c3533c66e3c1e7bc7974a2
https://doaj.org/article/1d2bd5275f844ba98289f769d1c30948
https://doaj.org/article/1d2bd5275f844ba98289f769d1c30948
Autor:
Katherine I. Kendig, Saurabh Baheti, Matthew A. Bockol, Travis M. Drucker, Steven N. Hart, Jacob R. Heldenbrand, Mikel Hernaez, Matthew E. Hudson, Michael T. Kalmbach, Eric W. Klee, Nathan R. Mattson, Christian A. Ross, Morgan Taschuk, Eric D. Wieben, Mathieu Wiepert, Derek E. Wildman, Liudmila S. Mainzer
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in Genetics
As reliable, efficient genome sequencing becomes ubiquitous, the need for similarly reliable and efficient variant calling becomes increasingly important. The Genome Analysis Toolkit (GATK), maintained by the Broad Institute, is currently the widely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4186210a316f67634f337bee35e4356a
https://www.frontiersin.org/article/10.3389/fgene.2019.00736/full
https://www.frontiersin.org/article/10.3389/fgene.2019.00736/full
Autor:
Matthew E. Hudson, Steven N. Hart, Katherine I Kendig, Michael T Kalmbach, Eric W. Klee, Mathieu Wiepert, Nathan R Mattson, Matthew A. Bockol, Derek E. Wildman, Travis M. Drucker, Jacob R Heldenbrand, Liudmila Sergeevna Mainzer, Eric D. Wieben, Saurabh Baheti, Ravishankar K. Iyer
Publikováno v:
BMC Bioinformatics
BMC Bioinformatics, Vol 20, Iss 1, Pp 1-9 (2019)
BMC Bioinformatics, Vol 20, Iss 1, Pp 1-9 (2019)
Background Use of the Genome Analysis Toolkit (GATK) continues to be the standard practice in genomic variant calling in both research and the clinic. Recently the toolkit has been rapidly evolving. Significant computational performance improvements
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::724a7092def1cb8f347a1e45e31de872
https://pubmed.ncbi.nlm.nih.gov/31847808
https://pubmed.ncbi.nlm.nih.gov/31847808
Autor:
Eric D. Wieben, Saurabh Baheti, Matthew A. Bockol, Jacob R Heldenbrand, Mathieu Wiepert, Eric W. Klee, Travis M. Drucker, Liudmila Sergeevna Mainzer, Nathan R Mattson, Steven N. Hart, Derek E. Wildman, Matthew E. Hudson, Mikel Hernaez, Katherine I Kendig, Michael T Kalmbach, Christian A. Ross, Morgan Taschuk
As reliable, efficient genome sequencing becomes more ubiquitous, the need for similarly reliable and efficient variant calling becomes increasingly important. The Genome Analysis Toolkit (GATK), maintained by the Broad Institute, is currently the wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d288965792ac62c9dc0530dd8dd654a
