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Peter Audano

dblp:148/0985 · DBLP profile ↗
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2ranked-venue papers
2as first author
0since 2021 · last 2018
0000-0002-5187-0415ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
variant calling
0.312018
Mapping-free variant calling using haplotype reconstruction from k-mer frequencies · Bioinform. 2018
Bioinformatics and computational biology
sequence analysis
0.322018
KAnalyze: a fast versatile pipelined K-mer toolkit · Bioinform. 2014
Mapping-free variant calling using haplotype reconstruction from k-mer frequencies · Bioinform. 2018
Bioinformatics and computational biology › sequence analysis › k-mer analysis
k-mer counting
0.212014
KAnalyze: a fast versatile pipelined K-mer toolkit · Bioinform. 2014
Bioinformatics and computational biology › sequence analysis
k-mer analysis
0.112018
Mapping-free variant calling using haplotype reconstruction from k-mer frequencies · Bioinform. 2018

Methods — techniques the papers use, named apart from their topics

k-mer frequency analysis · 0.3haplotype reconstruction · 0.3java · 0.2
YearPublicationVenuePosition
2018 Mapping-free variant calling using haplotype reconstruction from k-mer frequencies
abstract
Motivation: The standard protocol for detecting variation in DNA is to map millions of short sequence reads to a known reference and find loci that differ. While this approach works well, it cannot be applied where the sample contains dense variants or is too distant from known references. De novo assembly or hybrid methods can recover genomic variation, but the cost of computation is often much higher. We developed a novel k-mer algorithm and software implementation, Kestrel, capable of characterizing densely packed SNPs and large indels without mapping, assembly or de Bruijn graphs. Results: When applied to mosaic penicillin binding protein (PBP) genes in Streptococcus pneumoniae, we found near perfect concordance with assembled contigs at a fraction of the CPU time. Multilocus sequence typing (MLST) with this approach was able to bypass de novo assemblies. Kestrel has a very low false-positive rate when applied to the whole genome, and while Kestrel identified many variants missed by other methods, limitations of a purely k-mer based approach affect overall sensitivity. Availability and implementation: Source code and documentation for a Java implementation of Kestrel can be found at https://github.com/paudano/kestrel. All test code for this publication is located at https://github.com/paudano/kescases. Contact: [email protected] or [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online.
Peter Audano, Shashidhar Ravishankar, Fredrik Vannberg
Bioinform.1
2014 KAnalyze: a fast versatile pipelined K-mer toolkit
abstract
MOTIVATION: Converting nucleotide sequences into short overlapping fragments of uniform length, k-mers, is a common step in many bioinformatics applications. While existing software packages count k-mers, few are optimized for speed, offer an application programming interface (API), a graphical interface or contain features that make it extensible and maintainable. We designed KAnalyze to compete with the fastest k-mer counters, to produce reliable output and to support future development efforts through well-architected, documented and testable code. Currently, KAnalyze can output k-mer counts in a sorted tab-delimited file or stream k-mers as they are read. KAnalyze can process large datasets with 2 GB of memory. This project is implemented in Java 7, and the command line interface (CLI) is designed to integrate into pipelines written in any language. RESULTS: As a k-mer counter, KAnalyze outperforms Jellyfish, DSK and a pipeline built on Perl and Linux utilities. Through extensive unit and system testing, we have verified that KAnalyze produces the correct k-mer counts over multiple datasets and k-mer sizes. AVAILABILITY AND IMPLEMENTATION: KAnalyze is available on SourceForge: https://sourceforge.net/projects/kanalyze/.
Peter Audano, Fredrik Vannberg
Bioinform.1