FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads.
Pajuste, Fanny-Dhelia
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads. [electronic resource] - Scientific reports 05 2017 - 2537 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
2045-2322
10.1038/s41598-017-02487-5 doi
Algorithms
Bayes Theorem
Benchmarking
Genome, Human
Genotype
High-Throughput Nucleotide Sequencing
Humans
Polymorphism, Single Nucleotide
Reproducibility of Results
Sequence Analysis, DNA--methods
Software
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads. [electronic resource] - Scientific reports 05 2017 - 2537 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
2045-2322
10.1038/s41598-017-02487-5 doi
Algorithms
Bayes Theorem
Benchmarking
Genome, Human
Genotype
High-Throughput Nucleotide Sequencing
Humans
Polymorphism, Single Nucleotide
Reproducibility of Results
Sequence Analysis, DNA--methods
Software