Related references
Note: Only part of the references are listed.Quantitative prediction of the effect of genetic variation using hidden Markov models
Mingming Liu et al.
BMC BIOINFORMATICS (2014)
Accurate indel prediction using paired-end short reads
Dominik Grimm et al.
BMC GENOMICS (2013)
Analysis of insertion-deletion from deep-sequencing data: software evaluation for optimal detection
Joseph A. Neuman et al.
BRIEFINGS IN BIOINFORMATICS (2013)
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes
Stephen B. Montgomery et al.
GENOME RESEARCH (2013)
iRSpot-PseDNC: identify recombination spots with pseudo dinucleotide composition
Wei Chen et al.
NUCLEIC ACIDS RESEARCH (2013)
SIFT Indel: Predictions for the Functional Effects of Amino Acid Insertions/Deletions in Proteins
Jing Hu et al.
PLOS ONE (2013)
Prediction of replication origins by calculating DNA structural properties
Wei Chen et al.
FEBS LETTERS (2012)
Improved predictions of transcription factor binding sites using physicochemical features of DNA
Mark Maienschein-Cline et al.
NUCLEIC ACIDS RESEARCH (2012)
A Map of Minor Groove Shape and Electrostatic Potential from Hydroxyl Radical Cleavage Patterns of DNA
Eric P. Bishop et al.
ACS CHEMICAL BIOLOGY (2011)
Computational analysis suggests a highly bendable, fragile structure for nucleosomal DNA
Tadasu Nozaki et al.
GENE (2011)
Dindel: Accurate indel calls from short-read data
Cornelis A. Albers et al.
GENOME RESEARCH (2011)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo et al.
NATURE GENETICS (2011)
Impact of chromatin structure on sequence variability in the human genome
Michael Y. Tolstorukov et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)
Characterization and potential functional significance of human-chimpanzee large INDEL variation
Nalini Polavarapu et al.
MOBILE DNA (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
A time-invariant principle of genome evolution
Subhajyoti De et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
The role of DNA shape in protein-DNA recognition
Remo Rohs et al.
NATURE (2009)
Local DNA Topography Correlates with Functional Noncoding Regions of the Human Genome
Stephen C. J. Parker et al.
SCIENCE (2009)
The Human Gene Mutation Database: 2008 update
Peter D. Stenson et al.
GENOME MEDICINE (2009)
Generic eukaryotic core promoter prediction using structural features of DNA
Thomas Abeel et al.
GENOME RESEARCH (2008)
Construction of a genome-scale structural map at single-nucleotide resolution
Jason A. Greenbaum et al.
GENOME RESEARCH (2007)
Mechanism of a genetic glissando: structural biology of indel mutations
M Garcia-Diaz et al.
TRENDS IN BIOCHEMICAL SCIENCES (2006)
Influence of angiotensin converting enzyme insertion/deletion polymorphism on long-term total graft occlusion after coronary artery bypass surgery
SU Dayi et al.
HEART SURGERY FORUM (2005)
Mapping nucleic acid structure by hydroxyl radical cleavage
TD Tullius et al.
CURRENT OPINION IN CHEMICAL BIOLOGY (2005)
DNA replication fidelity
TA Kunkel
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Mobile elements: Drivers of genome evolution
HH Kazazian
SCIENCE (2004)
DNA sequence and comparative analysis of chimpanzee chromosome 22
H Watanabe et al.
NATURE (2004)
Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates
KA Frazer et al.
GENOME RESEARCH (2003)
Genome size reduction through illegitimate recombination counteracts genome expansion in Arabidopsis
KM Devos et al.
GENOME RESEARCH (2002)
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene
SMS Budde et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Share Paper
