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Stefan Kirov

dblp:32/5684 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2017
0000-0002-4650-1789ORCID · 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 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › functional genomics
CRISPR analysis
0.312017
CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline · Bioinform. 2017
Bioinformatics and computational biology
genomics
0.312017
CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline · Bioinform. 2017
Bioinformatics and computational biology › sequence analysis › sequence variation analysis
indel detection
0.312017
CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline · Bioinform. 2017
Bioinformatics and computational biology › genomics
next-generation sequencing data analysis
0.312017
CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline · Bioinform. 2017

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

burrows-wheeler aligner · 0.3assembly-based realignment · 0.3
YearPublicationVenuePosition
2017 CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline
abstract
SUMMARY: The simplicity and precision of CRISPR/Cas9 system has brought in a new era of gene editing. Screening for desired clones with CRISPR-mediated genomic edits in a large number of samples is made possible by next generation sequencing (NGS) due to its multiplexing. Here we present CRISPR-DAV (CRISPR Data Analysis and Visualization) pipeline to analyze the CRISPR NGS data in a high throughput manner. In the pipeline, Burrows-Wheeler Aligner and Assembly Based ReAlignment are used for small and large indel detection, and results are presented in a comprehensive set of charts and interactive alignment view. AVAILABILITY AND IMPLEMENTATION: CRISPR-DAV is available at GitHub and Docker Hub repositories: https://github.com/pinetree1/crispr-dav.git and https://hub.docker.com/r/pinetree1/crispr-dav/. CONTACT: [email protected].
Xuning Wang, Charles Tilford, Isaac Neuhaus, Gabe Mintier, John N. Feder, Stefan Kirov
Bioinform.7
2004 GOTree Machine (GOTM): a web-based platform for interpreting sets of interesting genes using Gene Ontology hierarchies
abstract
BACKGROUND: Microarray and other high-throughput technologies are producing large sets of interesting genes that are difficult to analyze directly. Bioinformatics tools are needed to interpret the functional information in the gene sets. RESULTS: We have created a web-based tool for data analysis and data visualization for sets of genes called GOTree Machine (GOTM). This tool was originally intended to analyze sets of co-regulated genes identified from microarray analysis but is adaptable for use with other gene sets from other high-throughput analyses. GOTree Machine generates a GOTree, a tree-like structure to navigate the Gene Ontology Directed Acyclic Graph for input gene sets. This system provides user friendly data navigation and visualization. Statistical analysis helps users to identify the most important Gene Ontology categories for the input gene sets and suggests biological areas that warrant further study. GOTree Machine is available online at http://genereg.ornl.gov/gotm/. CONCLUSION: GOTree Machine has a broad application in functional genomic, proteomic and other high-throughput methods that generate large sets of interesting genes; its primary purpose is to help users sort for interesting patterns in gene sets.
Bing Zhang 0003, Denise Schmoyer, Stefan Kirov, Jay Snoddy
BMC Bioinform.3