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Alicja Pacholewska

dblp:150/3233 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0002-4888-4883ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genomic data management
0.212014
SparkSeq: fast, scalable and cloud-ready tool for the interactive genomic data analysis with nucleotide precision · Bioinform. 2014
Bioinformatics and computational biology › genomics › genomic data analysis
interactive genomic data analysis
0.212014
SparkSeq: fast, scalable and cloud-ready tool for the interactive genomic data analysis with nucleotide precision · Bioinform. 2014
Bioinformatics and computational biology › genomics
next-generation sequencing data analysis
0.212014
SparkSeq: fast, scalable and cloud-ready tool for the interactive genomic data analysis with nucleotide precision · Bioinform. 2014

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

scala · 0.2mapreduce · 0.2apache spark · 0.2HDFS · 0.2
YearPublicationVenuePosition
2014 SparkSeq: fast, scalable and cloud-ready tool for the interactive genomic data analysis with nucleotide precision
abstract
UNLABELLED: Many time-consuming analyses of next -: generation sequencing data can be addressed with modern cloud computing. The Apache Hadoop-based solutions have become popular in genomics BECAUSE OF: their scalability in a cloud infrastructure. So far, most of these tools have been used for batch data processing rather than interactive data querying. The SparkSeq software has been created to take advantage of a new MapReduce framework, Apache Spark, for next-generation sequencing data. SparkSeq is a general-purpose, flexible and easily extendable library for genomic cloud computing. It can be used to build genomic analysis pipelines in Scala and run them in an interactive way. SparkSeq opens up the possibility of customized ad hoc secondary analyses and iterative machine learning algorithms. This article demonstrates its scalability and overall fast performance by running the analyses of sequencing datasets. Tests of SparkSeq also prove that the use of cache and HDFS block size can be tuned for the optimal performance on multiple worker nodes. AVAILABILITY AND IMPLEMENTATION: Available under open source Apache 2.0 license: https://bitbucket.org/mwiewiorka/sparkseq/.
Marek S. Wiewiórka, Antonio Messina, Alicja Pacholewska, Sergio Maffioletti, Piotr Gawrysiak, Michal J. Okoniewski
Bioinform.3