(Q42629171)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing (English)

1 reference

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18 January 2020

7

1 reference

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18 January 2020

Joke Reumers

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Peter De Rijk

2

1 reference

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Maarten J Van Den Bossche

18 January 2020

8

1 reference

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18 January 2020

Jurgen Del Favero

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

12

Ignace Vergote

1 reference

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18 January 2020

6

John Cleary

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

14

Diether Lambrechts

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

author name string

Hui Zhao

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Anthony Liekens

4

1 reference

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18 January 2020

Dominiek Smeets

5

1 reference

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18 January 2020

Kirsten Catthoor

9

1 reference

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18 January 2020

Bernard Sabbe

10

1 reference

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18 January 2020

Evelyn Despierre

11

1 reference

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18 January 2020

Brian Hilbush

13

1 reference

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18 January 2020

publication date

18 December 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

page(s)

61-68

1 reference

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https://scigraph.springernature.com/pub.10.1038/nbt.2053

18 January 2020

exact match

0 references

cites work

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1 reference

Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 January 2018

1 reference

A framework for variation discovery and genotyping using next-generation DNA sequencing data

21 January 2018

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21 January 2018

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21 January 2018

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Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

21 January 2018

1 reference

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

21 January 2018

1 reference

The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group

21 January 2018

1 reference

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

21 January 2018

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Accurate whole human genome sequencing using reversible terminator chemistry

21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

1 reference

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

21 January 2018

1 reference

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

21 January 2018

1 reference

The characterization of twenty sequenced human genomes

21 January 2018

1 reference

Ancient human genome sequence of an extinct Palaeo-Eskimo

21 January 2018

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Complete Khoisan and Bantu genomes from southern Africa

21 January 2018

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Sequencing and analysis of an Irish human genome

21 January 2018

1 reference

The complete genome of an individual by massively parallel DNA sequencing

21 January 2018

1 reference

The UCSC Genome Browser database: update 2010

21 January 2018

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A genome-wide view of the spectrum of spontaneous mutations in yeast.

21 January 2018

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Direct estimation of per nucleotide and genomic deleterious mutation rates in Drosophila

21 January 2018

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Distribution and intensity of constraint in mammalian genomic sequence

21 January 2018

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21 January 2018

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Recurrent copy number alterations in BRCA1-mutated ovarian tumors alter biological pathways.

21 January 2018

1 reference

Large-scale genomic analysis of ovarian carcinomas

21 January 2018

1 reference

A census of human cancer genes

21 January 2018

1 reference

Integrated genomic analyses of ovarian carcinoma

21 January 2018

1 reference

L1 retrotransposition in neurons is modulated by MeCP2.

21 January 2018

1 reference

Retroviral RNA identified in the cerebrospinal fluids and brains of individuals with schizophrenia

21 January 2018

1 reference

Integrating common and rare genetic variation in diverse human populations

21 January 2018

1 reference

Fast and accurate long-read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

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

21 January 2018

1 reference

novoSNP, a novel computational tool for sequence variation discovery

21 January 2018

1 reference

Allele-specific copy number analysis of tumors

21 January 2018

1 reference

TRANSFAC: an integrated system for gene expression regulation

21 January 2018

1 reference

ORegAnno: an open-access community-driven resource for regulatory annotation

21 January 2018

1 reference

VISTA Enhancer Browser--a database of tissue-specific human enhancers

21 January 2018

1 reference

A Hidden Markov Model approach to variation among sites in rate of evolution

21 January 2018

1 reference

SIFT: Predicting amino acid changes that affect protein function

21 January 2018

1 reference

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

CanPredict: a computational tool for predicting cancer-associated missense mutations

21 January 2018

1 reference

Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing

21 January 2018

1 reference

A highly annotated whole-genome sequence of a Korean individual

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22178994

12 December 2020

inferred from PubMed ID database lookup

The sequence is dead: long live the genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22178994

12 December 2020

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/22178994

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NBT.2053

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22178994%20AND%20SRC:MED&resulttype=core&format=json

release_tij2lkr7vzb7dedtq2cpd3y5va

18 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tij2lkr7vzb7dedtq2cpd3y5va

24 November 2022

mapped directly with Wikidata item

1 reference