(Q30758000)

26 June 2017

title

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls (English)

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26 June 2017

Justin M Zook

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Oliver Hofmann

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Oliver Hofmann

5

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Winston Hide

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Winston Hide

6

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David A. Mittelman

4

object named as

David Mittelman

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26 June 2017

Brad Chapman

2

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26 June 2017

Jason Wang

3

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26 June 2017

Marc Salit

7

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26 June 2017

publication date

16 February 2014

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26 June 2017

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26 June 2017

volume

32

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26 June 2017

issue

3

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26 June 2017

page(s)

246-251

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A comprehensive catalogue of somatic mutations from a human cancer genome

26 June 2017

cites work

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12 December 2020

First FDA authorization for next-generation sequencer

1 reference

12 December 2020

An integrated map of genetic variation from 1,092 human genomes

1 reference

12 December 2020

Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score

1 reference

12 December 2020

Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.

1 reference

12 December 2020

Comprehensive molecular characterization of human colon and rectal cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Accurate and comprehensive sequencing of personal genomes

1 reference

12 December 2020

The Sequence Alignment/Map format and SAMtools

1 reference

12 December 2020

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing.

1 reference

12 December 2020

Identification and correction of systematic error in high-throughput sequence data

1 reference

12 December 2020

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

1 reference

12 December 2020

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

1 reference

12 December 2020

Dissecting the genomic complexity underlying medulloblastoma

1 reference

12 December 2020

The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing

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12 December 2020

Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies

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12 December 2020

Single-nucleotide mutation rate increases close to insertions/deletions in eukaryotes.

1 reference

12 December 2020

Sequence analysis of mutations and translocations across breast cancer subtypes

1 reference

12 December 2020

A map of human genome variation from population-scale sequencing

1 reference

12 December 2020

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

12 December 2020

Synthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing

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12 December 2020

Performance comparison of whole-genome sequencing platforms

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12 December 2020

Characterizing and measuring bias in sequence data

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12 December 2020

Identifiers

DOI

10.1038/NBT.2835

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26 June 2017

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