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Federica Di Palma

dblp:52/8091 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0002-4394-0102ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2

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 8 heaviest of 9, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
comparative genomics
0.322014
The Naked Mole Rat Genome Resource: facilitating analyses of cancer and longevity-related adaptations · Bioinform. 2014
Genome-wide synteny through highly sensitive sequence alignment: Satsuma · Bioinform. 2010
Bioinformatics and computational biology
genome annotation
0.212014
The Naked Mole Rat Genome Resource: facilitating analyses of cancer and longevity-related adaptations · Bioinform. 2014
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly
0.212014
The Naked Mole Rat Genome Resource: facilitating analyses of cancer and longevity-related adaptations · Bioinform. 2014
Bioinformatics and computational biology › sequence alignment
genome alignment
0.112010
Genome-wide synteny through highly sensitive sequence alignment: Satsuma · Bioinform. 2010
Bioinformatics and computational biology › sequence alignment
maximal exact match
0.112010
Genome-wide synteny through highly sensitive sequence alignment: Satsuma · Bioinform. 2010
Bioinformatics and computational biology
sequence alignment
0.112010
Genome-wide synteny through highly sensitive sequence alignment: Satsuma · Bioinform. 2010
Bioinformatics and computational biology
sequence analysis
0.112010
Genome-wide synteny through highly sensitive sequence alignment: Satsuma · Bioinform. 2010
Bioinformatics and computational biology › sequence alignment › genome alignment
whole-genome alignment
0.112010
Genome-wide synteny through highly sensitive sequence alignment: Satsuma · Bioinform. 2010

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

sequence assembly · 0.2genome sequencing · 0.2fast fourier transform · 0.1cross-correlation · 0.1
YearPublicationVenuePosition
2014 The Naked Mole Rat Genome Resource: facilitating analyses of cancer and longevity-related adaptations
abstract
Abstract Motivation: The naked mole rat ( Heterocephalus glaber ) is an exceptionally long-lived and cancer-resistant rodent native to East Africa. Although its genome was previously sequenced, here we report a new assembly sequenced by us with substantially higher N50 values for scaffolds and contigs. Results: We analyzed the annotation of this new improved assembly and identified candidate genomic adaptations which may have contributed to the evolution of the naked mole rat’s extraordinary traits, including in regions of p53, and the hyaluronan receptors CD44 and HMMR (RHAMM). Furthermore, we developed a freely available web portal, the Naked Mole Rat Genome Resource ( http://www.naked-mole-rat.org ), featuring the data and results of our analysis, to assist researchers interested in the genome and genes of the naked mole rat, and also to facilitate further studies on this fascinating species. Availability and implementation: The Naked Mole Rat Genome Resource is freely available online at http://www.naked-mole-rat.org . This resource is open source and the source code is available at https://github.com/maglab/naked-mole-rat-portal . Contact: [email protected]
Thomas Craig, Jessica Alföldi, Aaron M. Berlin, Andrei Seluanov, Vera Gorbunova, Federica Di Palma, Kerstin Lindblad-Toh, George M. Church, João Pedro de Magalhães
Bioinform.8
2010 Genome-wide synteny through highly sensitive sequence alignment: Satsuma
abstract
MOTIVATION: Comparative genomics heavily relies on alignments of large and often complex DNA sequences. From an engineering perspective, the problem here is to provide maximum sensitivity (to find all there is to find), specificity (to only find real homology) and speed (to accommodate the billions of base pairs of vertebrate genomes). RESULTS: Satsuma addresses all three issues through novel strategies: (i) cross-correlation, implemented via fast Fourier transform; (ii) a match scoring scheme that eliminates almost all false hits; and (iii) an asynchronous 'battleship'-like search that allows for aligning two entire fish genomes (470 and 217 Mb) in 120 CPU hours using 15 processors on a single machine. AVAILABILITY: Satsuma is part of the Spines software package, implemented in C++ on Linux. The latest version of Spines can be freely downloaded under the LGPL license from http://www.broadinstitute.org/science/programs/genome-biology/spines/.
Manfred G. Grabherr, Pamela H. Russell, Miriah D. Meyer, Evan Mauceli, Jessica Alföldi, Federica Di Palma, Kerstin Lindblad-Toh
Bioinform.6