Evaluating Alignment and Variant-Calling Software for Mutation Identification in C. Elegans by Whole-Genome Sequencing

PLoS ONE - United States
doi 10.1371/journal.pone.0174446
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Public Library of Science (PLoS)

Related search

Empirical Evaluation of Variant Calling Accuracy Using Ultra-Deep Whole-Genome Sequencing Data

Scientific Reports
Multidisciplinary
2019English

Coval: Improving Alignment Quality and Variant Calling Accuracy for Next-Generation Sequencing Data

PLoS ONE
Multidisciplinary
2013English

Use of a Sibling Subtraction Method (SSM) for Identifying Causal Mutations in C. Elegans by Whole-Genome Sequencing

G3: Genes, Genomes, Genetics
MedicineGeneticsMolecular Biology
2017English

Comparison of Three Variant Callers for Human Whole Genome Sequencing

Scientific Reports
Multidisciplinary
2018English

Variant Detection Sensitivity and Biases in Whole Genome and Exome Sequencing

BMC Bioinformatics
BiochemistryApplied MathematicsComputer Science ApplicationsStructural BiologyMolecular Biology
2014English

Whole Genome Sequencing and Rare Variant Analysis in Essential Tremor Families

PLoS ONE
Multidisciplinary
2019English

Mapping Whole Genome Shotgun Sequence and Variant Calling in Mammalian Species Without Their Reference Genomes

F1000Research
GeneticsMolecular BiologyPharmacologyBiochemistryMicrobiology ImmunologyMedicineToxicologyPharmaceutics
2013English

Identification of Suppressors of MBK-2/Dyrk by Whole-Genome Sequencing

G3: Genes, Genomes, Genetics
MedicineGeneticsMolecular Biology
2013English

MethylExtract: High-Quality Methylation Maps and SNV Calling From Whole Genome Bisulfite Sequencing Data

F1000Research
GeneticsMolecular BiologyPharmacologyBiochemistryMicrobiology ImmunologyMedicineToxicologyPharmaceutics
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy