From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software (Q36668920)

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12 February 2020

title

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software (English)

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17

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Abdou ElSharawy

3

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Britt-Sabina Petersen

11

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16

Stefan Schreiber

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13

Espen Melum

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18

Andre Franke

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4

Georg Hemmrich

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author name string

Michael Forster

1

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12 February 2020

Peter Forster

2

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Benjamin Kreck

5

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Michael Wittig

6

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Ingo Thomsen

7

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Björn Stade

8

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Matthias Barann

9

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David Ellinghaus

10

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Sandra May

12

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Markus B Schilhabel

14

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Andreas Keller

15

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language of work or name

English

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publication date

10 September 2012

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12 February 2020

published in

Nucleic Acids Research

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volume

41

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12 February 2020

page(s)

e16

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issue

1

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Creative Commons Attribution-NonCommercial 3.0 Unported

12 February 2020

copyright license

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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PubMed

https://pubmed.ncbi.nlm.nih.gov/22965131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Increased exonic de novo mutation rate in individuals with schizophrenia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22965131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cancer. Heterogeneity and tumor history

1 reference

PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKS836

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22965131%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22965131%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22965131%20AND%20SRC:MED&resulttype=core&format=json