(Q64082800)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

title

A multi-task convolutional deep neural network for variant calling in single molecule sequencing (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

1 reference

convolutional neural network

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

Fritz Sedlazeck

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

author name string

Tak-Wah Lam

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

Michael C Schatz

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

language of work or name

English

0 references

publication date

1 March 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

published in

Nature Communications

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

page(s)

998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

26 April 2020

copyright license

start time

1 March 2019

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/s41467-019-09025-z

0 references

cites work

Coming of age: ten years of next-generation sequencing technologies

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Sequence-specific error profile of Illumina sequencers

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Benchmarking short sequence mapping tools

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Toward better understanding of artifacts in variant calling from high-coverage samples

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

16GT: a fast and sensitive variant caller using a 16-genotype probabilistic model

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Piercing the dark matter: bioinformatics of long-range sequencing and mapping.

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

A universal SNP and small-indel variant caller using deep neural networks

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

A map of human genome variation from population-scale sequencing

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

A complete bacterial genome assembled de novo using only nanopore sequencing data

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Joint variant and de novo mutation identification on pedigrees from high-throughput sequencing data

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Extensive sequencing of seven human genomes to characterize benchmark reference materials

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Skyhawk: An Artificial Neural Network-based discriminator for reviewing clinically significant genomic variants

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Improving SNP discovery by base alignment quality

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

A synthetic-diploid benchmark for accurate variant-calling evaluation

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Variant Review with the Integrative Genomics Viewer

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Oxford Nanopore MinION Sequencing and Genome Assembly

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Accurate detection of complex structural variations using single-molecule sequencing

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

Nanopore sequencing and assembly of a human genome with ultra-long reads.

1 reference

https://api.crossref.org/works/10.1038%2FS41467-019-09025-Z

7 January 2021

From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/30824707

12 December 2020

inferred from PubMed ID database lookup

Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/30824707

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/S41467-019-09025-Z

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

26 April 2020

ADS bibcode

2019NatCo..10..998L

0 references

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30824707%20AND%20SRC:MED&resulttype=core&format=json

26 April 2020

PubMed publication ID

30824707

1 reference