Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery. - Wikidata - wikimedia - TriplyDB

Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.

Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.

http://www.wikidata.org/entity/Q37529449

about

Using familial information for variant filtering in high-throughput sequencing studies Filtration and Normalization of Sequencing Read Data in Whole-Metagenome Shotgun Samples Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.Circulating tumor-derived DNA is shorter than somatic DNA in plasma.High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNA.Analytical Biases Associated with GC-Content in Molecular Evolution.Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens

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Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.

http://www.wikidata.org/entity/Q37529449

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 29 January 2014

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Investigating and correcting p ...... enhance aneuploidy discovery.

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Investigating and correcting p ...... enhance aneuploidy discovery.

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type

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Investigating and correcting p ...... enhance aneuploidy discovery.

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Investigating and correcting p ...... enhance aneuploidy discovery.

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prefLabel

Investigating and correcting p ...... enhance aneuploidy discovery.

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Investigating and correcting p ...... enhance aneuploidy discovery.

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JOURNAL.PONE.0086993

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Investigating and correcting p ...... enhance aneuploidy discovery.

@en

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Damien L Bruno

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Howard R Slater

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Melanie Bahlo

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Natalie P Thorne

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Yuval Benjamini

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P2860

Biases in Illumina transcriptome sequencing caused by random hexamer priming

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

The Sequence Alignment/Map format and SAMtools

Summarizing and correcting the GC content bias in high-throughput sequencing

Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing

Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.

Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma.

Personalized copy number and segmental duplication maps using next-generation sequencing.

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e86993

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scholarly article

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10.1371/JOURNAL.PONE.0086993

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1

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Devika Ganesamoorthy

Dineika Chandrananda

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260063345

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