Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications. [electronic resource]
Producer: 20150112Description: 912-918 p. digitalISSN:- 1546-1718
- Algorithms
- Chromosome Mapping -- methods
- Exome
- Genome, Human
- Genomic Structural Variation
- Genotype
- HLA Antigens -- genetics
- Haplotypes
- High-Throughput Nucleotide Sequencing -- methods
- Humans
- Mutation
- Polymorphism, Single Nucleotide
- Sensitivity and Specificity
- Sequence Analysis, DNA -- methods
- Software
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.