(Q33511017)

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Large scale single nucleotide polymorphism discovery in unsequenced genomes using second generation high throughput sequencing technology: applied to turkey

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scholarly article

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Europe PubMed Central

PubMed publication ID

27 July 2017

Large scale single nucleotide polymorphism discovery in unsequenced genomes using second generation high throughput sequencing technology: applied to turkey (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

high-throughput sequencing

1 reference

based on heuristic

inferred from title

Richard P. M. A. Crooijmans

2

object named as

Richard P M A Crooijmans

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Hindrik H D Kerstens

1

object named as

Hindrik H D Kerstens

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Martien Groenen

7

object named as

Martien A M Groenen

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

author name string

Albertine Veenendaal

3

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Bert W Dibbits

4

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Thomas F C Chin-A-Woeng

5

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Johan T den Dunnen

6

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Europe PubMed Central

PubMed publication ID

27 July 2017

language of work or name

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publication date

16 October 2009

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Europe PubMed Central

PubMed publication ID

27 July 2017

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Europe PubMed Central

PubMed publication ID

27 July 2017

10

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Europe PubMed Central

PubMed publication ID

27 July 2017

479

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

1 reference

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21 June 2018

Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

1 reference

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21 June 2018

The YH database: the first Asian diploid genome database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Mapping short DNA sequencing reads and calling variants using mapping quality scores

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

The new paradigm of flow cell sequencing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Association and in silico assignment of sequences from turkey BACs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Whole genome comparative studies between chicken and turkey and their implications for avian genome evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Velvet: algorithms for de novo short read assembly using de Bruijn graphs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

ALLPATHS: de novo assembly of whole-genome shotgun microreads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Short read fragment assembly of bacterial genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

How repetitive are genomes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

A high-density screen for linkage in multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Human-mouse alignments with BLASTZ

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Complex SNP-based haplotypes in three human helicases: implications for cancer association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

An SNP map of the human genome generated by reduced representation shotgun sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

A greedy algorithm for aligning DNA sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

21 June 2018

Assembling millions of short DNA sequences using SSAKE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

31 October 2018

De novoassembly of thePseudomonas syringaepv.syringaeB728a genome using Illumina/Solexa short sequence reads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772860

31 October 2018

Using the chicken genome sequence in the development and mapping of genetic markers in the turkey (Meleagris gallopavo)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19835600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP discovery in swine by reduced representation and high throughput pyrosequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/19835600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2164-10-479

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-10-479

9 September 2019

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

ResearchGate publication ID

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