Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.
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Using familial information for variant filtering in high-throughput sequencing studiesFiltration and Normalization of Sequencing Read Data in Whole-Metagenome Shotgun SamplesNovel 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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P2860
Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.
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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.
@en
Investigating and correcting p ...... enhance aneuploidy discovery.
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Investigating and correcting p ...... enhance aneuploidy discovery.
@en
Investigating and correcting p ...... enhance aneuploidy discovery.
@nl
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Investigating and correcting p ...... enhance aneuploidy discovery.
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Damien L Bruno
Howard R Slater
Melanie Bahlo
Natalie P Thorne
Yuval Benjamini
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P304
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10.1371/JOURNAL.PONE.0086993
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P577
2014-01-29T00:00:00Z