Species-independent identification of known and novel recurrent genomic entities in multiple cancer patients

Jens Friis-Nielsen; Jose Maria Gonzalez-Izarzugaza; Søren Brunak

doi:10.1186/s40246-016-0063-5

Species-independent identification of known and novel recurrent genomic entities in multiple cancer patients

Jens Friis-Nielsen, Jose Maria Gonzalez-Izarzugaza, Søren Brunak

Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

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Abstract

Here we present a new method for the identification of recurrent genomic entities that play a causative role in the onset of disease. Our approach is particularly amenable for the analyses highthroughput sequencing data.

Original language	English
Article number	P16
Journal	Human Genomics (Online)
Volume	10
Issue number	Suppl. 1
ISSN	1479-7364
DOIs	https://doi.org/10.1186/s40246-016-0063-5
Publication status	Published - 2016
Event	Human Genome Meeting 2016 - Houston, TX, United States Duration: 28 Feb 2016 → 2 Mar 2016

Conference

Conference	Human Genome Meeting 2016
Country/Territory	United States
City	Houston, TX
Period	28/02/2016 → 02/03/2016

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1186/s40246-016-0063-5

HumanGenomicsFinal published version, 2.05 MB

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title = "Species-independent identification of known and novel recurrent genomic entities in multiple cancer patients",

abstract = "Here we present a new method for the identification of recurrent genomic entities that play a causative role in the onset of disease. Our approach is particularly amenable for the analyses highthroughput sequencing data.",

author = "Jens Friis-Nielsen and Gonzalez-Izarzugaza, {Jose Maria} and S{\o}ren Brunak",

year = "2016",

doi = "10.1186/s40246-016-0063-5",

language = "English",

volume = "10",

journal = "Human Genomics (Online)",

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T1 - Species-independent identification of known and novel recurrent genomic entities in multiple cancer patients

AU - Friis-Nielsen, Jens

AU - Gonzalez-Izarzugaza, Jose Maria

AU - Brunak, Søren

PY - 2016

Y1 - 2016

N2 - Here we present a new method for the identification of recurrent genomic entities that play a causative role in the onset of disease. Our approach is particularly amenable for the analyses highthroughput sequencing data.

AB - Here we present a new method for the identification of recurrent genomic entities that play a causative role in the onset of disease. Our approach is particularly amenable for the analyses highthroughput sequencing data.

U2 - 10.1186/s40246-016-0063-5

DO - 10.1186/s40246-016-0063-5

M3 - Conference abstract in journal

C2 - 27294413

VL - 10

JO - Human Genomics (Online)

JF - Human Genomics (Online)

SN - 1479-7364

IS - Suppl. 1

M1 - P16

T2 - Human Genome Meeting 2016

Y2 - 28 February 2016 through 2 March 2016

ER -

Species-independent identification of known and novel recurrent genomic entities in multiple cancer patients

Abstract

Conference

UN SDGs

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