(Q35541141)

8 August 2017

title

A Bayesian framework for de novo mutation calling in parents-offspring trios (English)

1 reference

8 August 2017

Qiang Wei

1

1 reference

8 August 2017

Xiaowei Zhan

2

1 reference

8 August 2017

Xue Zhong

3

1 reference

8 August 2017

Yongzhuang Liu

4

1 reference

8 August 2017

Yujun Han

5

1 reference

8 August 2017

Wei Chen

6

1 reference

8 August 2017

Bingshan Li

7

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8 August 2017

language of work or name

English

0 references

publication date

21 December 2014

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8 August 2017

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8 August 2017

volume

31

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8 August 2017

issue

9

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8 August 2017

page(s)

1375-1381

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A gradient-boosting approach for filtering de novo mutations in parent-offspring trios

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

De novo mutations in schizophrenia implicate synaptic networks

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

The role of de novo mutations in the genetics of autism spectrum disorders

12 July 2018

1 reference

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DeNovoGear: de novo indel and point mutation discovery and phasing.

12 July 2018

1 reference

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Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network

12 July 2018

1 reference

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De novo mutations in the genome organizer CTCF cause intellectual disability.

12 July 2018

1 reference

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A likelihood-based framework for variant calling and de novo mutation detection in families

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Estimating the human mutation rate using autozygosity in a founder population

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

De Novo Gene Disruptions in Children on the Autistic Spectrum

12 July 2018

1 reference

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

12 July 2018

1 reference

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

12 July 2018

1 reference

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Variation in genome-wide mutation rates within and between human families

12 July 2018

1 reference

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Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

12 July 2018

1 reference

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The variant call format and VCFtools

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Genotype and SNP calling from next-generation sequencing data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

12 July 2018

1 reference

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia

12 July 2018

1 reference

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

The Sequence Alignment/Map format and SAMtools

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Fast and accurate short read alignment with Burrows-Wheeler transform

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

Strong association of de novo copy number mutations with autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

A de novo paradigm for mental retardation.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4410659

10.1093/BIOINFORMATICS/BTU839

26 September 2018

Identifiers

DOI

1 reference

journals/bioinformatics/WeiZZLHCL15

8 August 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

8 August 2017

1 reference