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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools.
Published in:
Nucleic Acids Research, 2013, v. 41, p. D94, doi. 10.1093/nar/gks955
By:
- Cer, Regina Z.;
- Donohue, Duncan E.;
- Mudunuri, Uma S.;
- Temiz, Nuri A.;
- Loss, Michael A.;
- Starner, Nathan J.;
- Halusa, Goran N.;
- Volfovsky, Natalia;
- Ming Yi;
- Luke, Brian T.;
- Bacolla, Albino;
- Collins, Jack R.;
- Stephens, Robert M.
Publication type:
Article
Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes.
Published in:
Nucleic Acids Research, 2011, v. 39, n. suppl_1, p. D383, doi. 10.1093/nar/gkq1170
By:
- Cer, Regina Z.;
- Bruce, Kevin H.;
- Mudunuri, Uma S.;
- Yi, Ming;
- Volfovsky, Natalia;
- Luke, Brian T.;
- Bacolla, Albino;
- Collins, Jack R.;
- Stephens, Robert M.
Publication type:
Article
AVIA 3.0: interactive portal for genomic variant and sample level analysis.
Published in:
Bioinformatics, 2021, v. 37, n. 16, p. 2467, doi. 10.1093/bioinformatics/btaa994
By:
- Reardon, Hue V;
- Che, Anney;
- Luke, Brian T;
- Ravichandran, Sarangan;
- Collins, Jack R;
- Mudunuri, Uma S
Publication type:
Article
Knowledge and Theme Discovery across Very Large Biological Data Sets Using Distributed Queries: A Prototype Combining Unstructured and Structured Data.
Published in:
PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0080503
By:
- Mudunuri, Uma S.;
- Khouja, Mohamad;
- Repetski, Stephen;
- Venkataraman, Girish;
- Che, Anney;
- Luke, Brian T.;
- Girard, F. Pascal;
- Stephens, Robert M.
Publication type:
Article
Rare disease variant curation from literature: assessing gaps with creatine transport deficiency in focus.
Published in:
BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-023-09561-5
By:
- Lyons, Erica L.;
- Watson, Daniel;
- Alodadi, Mohammad S.;
- Haugabook, Sharie J.;
- Tawa, Gregory J.;
- Hannah-Shmouni, Fady;
- Porter, Forbes D.;
- Collins, Jack R.;
- Ottinger, Elizabeth A.;
- Mudunuri, Uma S.
Publication type:
Article
Guanine Holes Are Prominent Targets for Mutation in Cancer and Inherited Disease.
Published in:
PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003816
By:
- Bacolla, Albino;
- Temiz, Nuri A.;
- Yi, Ming;
- Ivanic, Joseph;
- Cer, Regina Z.;
- Donohue, Duncan E.;
- Ball, Edward V.;
- Mudunuri, Uma S.;
- Wang, Guliang;
- Jain, Aklank;
- Volfovsky, Natalia;
- Luke, Brian T.;
- Stephens, Robert M.;
- Cooper, David N.;
- Collins, Jack R.;
- Vasquez, Karen M.
Publication type:
Article
AVIA v2.0: annotation, visualization and impact analysis of genomic variants and genes.
Published in:
2015
By:
- Hue Vuong;
- Anney Che;
- Ravichandran, Sarangan;
- Luke, Brian T.;
- Collins, Jack R.;
- Mudunuri, Uma S.
Publication type:
Product Review

Found: 7

Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools.

Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes.

AVIA 3.0: interactive portal for genomic variant and sample level analysis.

Knowledge and Theme Discovery across Very Large Biological Data Sets Using Distributed Queries: A Prototype Combining Unstructured and Structured Data.

Rare disease variant curation from literature: assessing gaps with creatine transport deficiency in focus.

Guanine Holes Are Prominent Targets for Mutation in Cancer and Inherited Disease.

AVIA v2.0: annotation, visualization and impact analysis of genomic variants and genes.