Determining Multiallelic Complex Copy Number and Sequence Variation From High Coverage Exome Sequencing Data

BMC Genomics - United Kingdom
doi 10.1186/s12864-015-2123-y
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Estimation of Copy Number Alterations From Exome Sequencing Data

PLoS ONE
Multidisciplinary
2012English

Correction: CoNVEX: Copy Number Variation Estimation in Exome Sequencing Data Using HMM

BMC Bioinformatics
BiochemistryApplied MathematicsComputer Science ApplicationsStructural BiologyMolecular Biology
2013English

An Evaluation of Copy Number Variation Detection Tools for Cancer Using Whole Exome Sequencing Data

BMC Bioinformatics
BiochemistryApplied MathematicsComputer Science ApplicationsStructural BiologyMolecular Biology
2017English

A Sparse Model Based Detection of Copy Number Variations From Exome Sequencing Data

IEEE Transactions on Biomedical Engineering
Biomedical Engineering
2016English

cnvHiTSeq: Integrative Models for High-Resolution Copy Number Variation Detection and Genotyping Using Population Sequencing Data

Genome Biology
2012English

162 Combinatorial Analysis of Exome Sequencing Data and Copy Number Variants in Congenital Heart Disease Patients

Heart
Cardiovascular MedicineCardiology
2017English

Detection of Copy Number Variations in Epilepsy Using Exome Data

Clinical Genetics
Genetics
2018English

A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing

PLoS ONE
Multidisciplinary
2013English

A Distance-Type Measure Approach to the Analysis of Copy Number Variation in DNA Sequencing Data

BMC Genomics
BiotechnologyGenetics
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy