(Q41197442)

28 September 2017

novoSNP, a novel computational tool for sequence variation discovery (English)

1 reference

Christine Van Broeckhoven

28 September 2017

7

object named as

Christine Van Broeckhoven

0 references

Peter De Rijk

object named as

Peter De Rijk

8

0 references

Rosa Rademakers

3

object named as

Rosa Rademakers

1 reference

28 September 2017

Stefan Weckx

1

1 reference

28 September 2017

Jurgen Del-Favero

2

1 reference

28 September 2017

Lieve Claes

4

1 reference

28 September 2017

Marc Cruts

5

1 reference

28 September 2017

Peter De Jonghe

6

1 reference

28 September 2017

1 March 2005

1 reference

28 September 2017

1 reference

28 September 2017

15

1 reference

28 September 2017

3

1 reference

28 September 2017

436-442

1 reference

describes a project that uses

28 September 2017

SQL

1 reference

26 June 2022

https://europepmc.org/article/PMC/PMC551570

based on heuristic

inferred from PubMed Central ID database lookup

cites work

SNPbox: a modular software package for large-scale primer design

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

SNPbox: web-based high-throughput primer design from gene to genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

HGVbase: a curated resource describing human DNA variation and phenotype relationships

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Initial sequencing and comparative analysis of the mouse genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Initial sequencing and analysis of the human genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

The Sequence of the Human Genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

dbSNP: the NCBI database of genetic variation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

The genome sequence of Drosophila melanogaster

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Genome sequence of the nematode C. elegans: a platform for investigating biology

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Base-calling of automated sequencer traces using phred. II. Error probabilities

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Basic local alignment search tool

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

A general approach to single-nucleotide polymorphism discovery.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

Comparative Analysis of Human DNA Variations by Fluorescence-Based Sequencing of PCR Products

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=551570

2 December 2018

Identifiers

DOI

10.1101/GR.2754005

1 reference

28 September 2017

1 reference

28 September 2017

PubMed publication ID

15741513

1 reference