ORIGINAL RESEARCH
Published on 12 Aug 2014
A hidden Markov model for haplotype inference for present-absent data of clustered genes using identified haplotypes and haplotype patterns
doi 10.3389/fgene.2014.00267
- 3,793 views
- 1 citation
- Frontiers in Genetics
- Statistical Genetics and Methodology
- Research Topics
- Statistical method for CNV detection and disease association
Statistical method for CNV detection and disease association
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Articles
METHODS
Published on 18 Mar 2014
VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions
doi 10.3389/fgene.2014.00053
- 3,739 views
- 2 citations
ORIGINAL RESEARCH
Published on 28 Oct 2013
Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight
doi 10.3389/fgene.2013.00196
- 3,560 views
- 17 citations
ORIGINAL RESEARCH
Published on 25 Oct 2013
Evaluation of calling algorithms for array-CGH
doi 10.3389/fgene.2013.00217
- 4,126 views
- 11 citations
METHODS
Published on 23 Sep 2013
A method for calling copy number polymorphism using haplotypes
doi 10.3389/fgene.2013.00165
- 4,440 views
- 2 citations
ORIGINAL RESEARCH
Published on 23 Sep 2013
A stochastic inference of de novo CNV detection and association test in multiplex schizophrenia families
doi 10.3389/fgene.2013.00185
- 3,412 views
REVIEW
Published on 26 Aug 2013
The Role and Challenges of Exome Sequencing in Studies of Human Diseases
doi 10.3389/fgene.2013.00160
- 14,601 views
- 83 citations
METHODS
Published on 16 Aug 2013
MATCHCLIP: locate precise breakpoints for copy number variation using CIGAR string by matching soft clipped reads
doi 10.3389/fgene.2013.00157
- 6,655 views
- 17 citations
REVIEW
Published on 30 May 2013
The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation
doi 10.3389/fgene.2013.00092
- 16,065 views
- 54 citations
Published in
Frontiers in Genetics
- Statistical Genetics and Methodology
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- 57kTopic views
- 41kArticle views
- 12kArticle downloads