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Pedro J. Torres

dblp:86/7045 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2017
0000-0002-1243-7440ORCID · conflict

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
metagenomics
0.312017
PARTIE: a partition engine to separate metagenomic and amplicon projects in the Sequence Read Archive · Bioinform. 2017
Bioinformatics and computational biology › sequence analysis › sequence classification
read classification
0.312017
PARTIE: a partition engine to separate metagenomic and amplicon projects in the Sequence Read Archive · Bioinform. 2017

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

random forest · 0.3k-mer frequency · 0.3
YearPublicationVenuePosition
2017 PARTIE: a partition engine to separate metagenomic and amplicon projects in the Sequence Read Archive
abstract
MOTIVATION: The Sequence Read Archive (SRA) contains raw data from many different types of sequence projects. As of 2017, the SRA contained approximately ten petabases of DNA sequence (10 16 bp). Annotations of the data are provided by the submitter, and mining the data in the SRA is complicated by both the amount of data and the detail within those annotations. Here, we introduce PARTIE, a partition engine optimized to differentiate sequence read data into metagenomic (random) and amplicon (targeted) sequence data sets. RESULTS: PARTIE subsamples reads from the sequencing file and calculates four different statistics: k -mer frequency, 16S abundance, prokaryotic- and viral-read abundance. These metrics are used to create a RandomForest decision tree to classify the sequencing data, and PARTIE provides mechanisms for both supervised and unsupervised classification. We demonstrate the accuracy of PARTIE for classifying SRA data, discuss the probable error rates in the SRA annotations and introduce a resource assessing SRA data. AVAILABILITY AND IMPLEMENTATION: PARTIE and reclassified metagenome SRA entries are available from https://github.com/linsalrob/partie. CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Pedro J. Torres, Robert A. Edwards, Katelyn McNair
Bioinform.1