Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.

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Enhancing Next-Generation Sequencing-Guided Cancer Care Through Cognitive Computing.Cell-free DNA: Treasure trove for cancer medicine.2017 Year in Review and Message from the Editors to Our Reviewers.

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Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.

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Comparing sequencing assays an ...... ble genomics for glioblastoma.

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Comparing sequencing assays an ...... ble genomics for glioblastoma.

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Andrew B Lassman

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Anne-Katrin Emde

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Bo-Juen Chen

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Christian Grommes

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Erhan Bilal

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Ewa A Bergmann

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Jeffrey N Bruce

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Julia L Moore Vogel

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Kahn Rhrissorrakrai

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DELLY: structural variant discovery by integrated paired-end and split-read analysis

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

Fast and accurate short read alignment with Burrows-Wheeler transform

A global reference for human genetic variation

Activation of MET via diverse exon 14 splicing alterations occurs in multiple tumor types and confers clinical sensitivity to MET inhibitors.

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Mutational landscape and significance across 12 major cancer types

Organizing knowledge to enable personalization of medicine in cancer

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3

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Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.

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Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.

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