[HTML] springer.comFull View

[HTML][HTML] SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru, B Schmidt - BMC Systems Biology, 2016 - Springer
Background Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …
被引用次数：44 相关文章

SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.

Y Liu, M Loewer, S Aluru, B Schmidt - BMC Systems Biology, 2016 - search.ebscohost.com
Background: Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …
[PDF] researchgate.net

[PDF][PDF] SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru, B Schmidt - 2016 - researchgate.net
Background: Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …
[HTML] nih.gov

[HTML][HTML] SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru, B Schmidt - BMC Systems Biology, 2016 - ncbi.nlm.nih.gov
Background Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …

SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.

Y Liu, M Loewer, S Aluru, B Schmidt - BMC Systems Biology, 2016 - europepmc.org
Background Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …

SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru… - BMC systems …, 2016 - pubmed.ncbi.nlm.nih.gov
Background Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …
[PDF] core.ac.uk

[PDF][PDF] SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru, B Schmidt - 2016 - core.ac.uk
Background: Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …

SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru, B Schmidt - BMC Systems Biology, 2016 - go.gale.com
Background Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …
[HTML] biomedcentral.com

[HTML][HTML] SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru… - BMC Systems …, 2016 - bmcsystbiol.biomedcentral.com
Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-deletion
(indel) mutations have been developed based on next-generation sequencing (NGS) …

SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

Y Liu, M Loewer, S Aluru, B Schmidt - BMC Systems Biology, 2016 - infona.pl
Background Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-
deletion (indel) mutations have been developed based on next-generation sequencing …