David N. Cooper

According to our database1, David N. Cooper authored at least 17 papers between 1998 and 2018.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Other 

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Bibliography

2018
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.
Bioinformatics, 2018

2017
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.
BMC Bioinformatics, 2017

When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.
Bioinformatics, 2017

2016
The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease.
PLoS Computational Biology, 2016

Mining clinical attributes of genomic variants through assisted literature curation in Egas.
Database, 2016

2015
An integrative approach to predicting the functional effects of non-coding and coding sequence variation.
Bioinformatics, 2015

DDIG-in: detecting disease-causing genetic variations due to frameshifting indels and nonsense mutations employing sequence and structural properties at nucleotide and protein levels.
Bioinformatics, 2015

Sequential data selection for predicting the pathogenic effects of sequence variation.
Proceedings of the 2015 IEEE International Conference on Bioinformatics and Biomedicine, 2015

2014
A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing.
PLoS Computational Biology, 2014

2013
Predicting the functional consequences of cancer-associated amino acid substitutions.
Bioinformatics, 2013

CRAVAT: cancer-related analysis of variants toolkit.
Bioinformatics, 2013

2012
regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions.
Bioinformatics, 2012

2010
Structure-based kernels for the prediction of catalytic residues and their involvement in human inherited disease.
BMC Bioinformatics, 2010

Structure-based kernels for the prediction of catalytic residues and their involvement in human inherited disease.
Bioinformatics, 2010

2009
Automated inference of molecular mechanisms of disease from amino acid substitutions.
Bioinformatics, 2009

2006
In Silico Discrimination of Single Nucleotide Polymorphisms and Pathological Mutations in Human Gene Promoter Regions by Means of Local DNA Sequence Context and Regularity.
In Silico Biology, 2006

1998
The human gene mutation database.
Nucleic Acids Research, 1998


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