Deep sequencing to reveal new variants in pooled DNA samples (Q44639856)

4 December 2017

Deep sequencing to reveal new variants in pooled DNA samples (English)

1 reference

4 December 2017

7

1 reference

4 December 2017

Jelle J Goeman

3

0 references

Stephan Ossowski

object named as

Stephan Ossowski

5

0 references

Peter Devilee

14

object named as

Peter Devilee

1 reference

4 December 2017

Astrid A Out

1

1 reference

4 December 2017

Ivonne J H M van Minderhout

2

1 reference

4 December 2017

Yavuz Ariyurek

4

1 reference

4 December 2017

Korbinian Schneeberger

6

1 reference

4 December 2017

Michiel van Galen

8

1 reference

4 December 2017

Peter E M Taschner

9

1 reference

4 December 2017

Carli M J Tops

10

1 reference

4 December 2017

Martijn H Breuning

11

1 reference

4 December 2017

Gert-Jan B van Ommen

12

1 reference

4 December 2017

Johan T den Dunnen

13

1 reference

4 December 2017

Frederik J Hes

15

1 reference

4 December 2017

1 December 2009

1 reference

4 December 2017

1 reference

4 December 2017

30

1 reference

4 December 2017

12

1 reference

4 December 2017

1703-1712

1 reference

Direct selection of human genomic loci by microarray hybridization

4 December 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Targeted next-generation sequencing by specific capture of multiple genomic loci using low-volume microfluidic DNA arrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Accurate whole human genome sequencing using reversible terminator chemistry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Common and rare variants in multifactorial susceptibility to common diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

MUTYH-associated polyposis--from defect in base excision repair to clinical genetic testing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Standardizing mutation nomenclature: why bother?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Quantification of rare allelic variants from pooled genomic DNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Real-time DNA sequencing from single polymerase molecules

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Amino acid difference formula to help explain protein evolution

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Method for improving sequence coverage uniformity of targeted genomic intervals amplified by LR-PCR using Illumina GA sequencing-by-synthesis technology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Genome-wide significance for dense SNP and resequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

The search for low-penetrance cancer susceptibility alleles

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

SNP frequency estimation using massively parallel sequencing of pooled DNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

DNA sequencing. A plan to capture human diversity in 1000 genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

The thorough screening of the MUTYH gene in a large French cohort of sporadic colorectal cancers.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Parallel tagged sequencing on the 454 platform

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

T-Coffee: A novel method for fast and accurate multiple sequence alignment

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Sequencing of natural strains of Arabidopsis thaliana with short reads

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

A pyrosequencing-tailored nucleotide barcode design unveils opportunities for large-scale sample multiplexing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Generations of sequencing technologies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Parallel sequencing used in detection of mosaic mutations: comparison with four diagnostic DNA screening techniques.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

New perspectives for the elucidation of genetic disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Low-abundance drug-resistant viral variants in chronically HIV-infected, antiretroviral treatment-naive patients significantly impact treatment outcomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

A comparison of bayesian methods for haplotype reconstruction from population genotype data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Characterization of mutation spectra with ultra-deep pyrosequencing: application to HIV-1 drug resistance

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Extension of Lander-Waterman theory for sequencing filtered DNA libraries.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Aspects of coverage in medical DNA sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21122

7 January 2021

Identifiers

DOI

10.1002/HUMU.21122

1 reference

4 December 2017

1 reference