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Carolina Dallett

dblp:70/7237 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2016
0000-0002-6034-1099ORCID · 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
1 paper
Bioinformatics and computational biology · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
sequencing simulation
0.212016
LongISLND: in silico sequencing of lengthy and noisy datatypes · Bioinform. 2016
Bioinformatics and computational biology › genomics
variant calling
0.112016
LongISLND: in silico sequencing of lengthy and noisy datatypes · Bioinform. 2016

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

consensus building · 0.2
YearPublicationVenuePosition
2016 LongISLND: in silico sequencing of lengthy and noisy datatypes
abstract
LongISLND is a software package designed to simulate sequencing data according to the characteristics of third generation, single-molecule sequencing technologies. The general software architecture is easily extendable, as demonstrated by the emulation of Pacific Biosciences (PacBio) multi-pass sequencing with P5 and P6 chemistries, producing data in FASTQ, H5, and the latest PacBio BAM format. We demonstrate its utility by downstream processing with consensus building and variant calling. AVAILABILITY AND IMPLEMENTATION: LongISLND is implemented in Java and available at http://bioinform.github.io/longislnd CONTACT: [email protected] information: Supplementary data are available at Bioinformatics online.
Bayo Lau, Marghoob Mohiyuddin, John C. Mu, Li Tai Fang, Narges Bani Asadi, Carolina Dallett, Hugo Y. K. Lam
Bioinform.6
2009 ResBoost: characterizing and predicting catalytic residues in enzymes
abstract
BACKGROUND: Identifying the catalytic residues in enzymes can aid in understanding the molecular basis of an enzyme's function and has significant implications for designing new drugs, identifying genetic disorders, and engineering proteins with novel functions. Since experimentally determining catalytic sites is expensive, better computational methods for identifying catalytic residues are needed. RESULTS: We propose ResBoost, a new computational method to learn characteristics of catalytic residues. The method effectively selects and combines rules of thumb into a simple, easily interpretable logical expression that can be used for prediction. We formally define the rules of thumb that are often used to narrow the list of candidate residues, including residue evolutionary conservation, 3D clustering, solvent accessibility, and hydrophilicity. ResBoost builds on two methods from machine learning, the AdaBoost algorithm and Alternating Decision Trees, and provides precise control over the inherent trade-off between sensitivity and specificity. We evaluated ResBoost using cross-validation on a dataset of 100 enzymes from the hand-curated Catalytic Site Atlas (CSA). CONCLUSION: ResBoost achieved 85% sensitivity for a 9.8% false positive rate and 73% sensitivity for a 5.7% false positive rate. ResBoost reduces the number of false positives by up to 56% compared to the use of evolutionary conservation scoring alone. We also illustrate the ability of ResBoost to identify recently validated catalytic residues not listed in the CSA.
Ron Alterovitz, Aaron Arvey, Sriram Sankararaman, Carolina Dallett, Yoav Freund, Kimmen Sjölander
BMC Bioinform.4