Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer (Q33374628)

26 July 2017

title

Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer (English)

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26 July 2017

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Raoul Bonnal

2

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Sara Benedetti

Sara Benedetti

5

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Ermanno Rizzi

Ermanno Rizzi

3

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Gianluca De Bellis

Gianluca De Bellis

14

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Alberto Albertini

Alberto Albertini

11

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Roberta Bordoni

1

Roberta Bordoni

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26 July 2017

12

Luigi Rossi Bernardi

1 reference

26 July 2017

Paola Carrera

4

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26 July 2017

Laura Cremonesi

6

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26 July 2017

Stefania Stenirri

7

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26 July 2017

Alessio Colombo

8

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26 July 2017

Cristina Montrasio

9

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26 July 2017

Sara Bonalumi

10

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26 July 2017

Maurizio Ferrari

13

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26 July 2017

language of work or name

English

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publication date

8 October 2008

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26 July 2017

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26 July 2017

volume

9

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26 July 2017

page(s)

464

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describes a project that uses

26 July 2017

SQL

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26 June 2022

https://europepmc.org/article/PMC/PMC2569949

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Genome-wide in situ exon capture for selective resequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Multiplex amplification of large sets of human exons

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Direct selection of human genomic loci by microarray hybridization

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

The genomic landscapes of human breast and colorectal cancers

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Multigene amplification and massively parallel sequencing for cancer mutation discovery

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Unexplained neonatal respiratory distress due to congenital surfactant deficiency

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

The use of coded PCR primers enables high-throughput sequencing of multiple homolog amplification products by 454 parallel sequencing

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

The consensus coding sequences of human breast and colorectal cancers

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Accurate multiplex polony sequencing of an evolved bacterial genome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Genome sequencing in microfabricated high-density picolitre reactors

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Sequence information can be obtained from single DNA molecules

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Genetic heterogeneity in Italian families with familial hemiplegic migraine

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

A sequencing method based on real-time pyrophosphate

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Basic local alignment search tool

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Genetic and clinical heterogeneity of ferroportin disease.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Beta-thalassemia microelectronic chip: a fast and accurate method for mutation detection.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Accessing genetic information with high-density DNA arrays.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569949

Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18842124

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-9-464

1 reference

Dimensions Publication ID

26 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-9-464

9 September 2019

1 reference

26 July 2017

1 reference