M2SG: mapping human disease-related genetic variants to protein sequences and genomic loci.
Renkai JiQian CongWenlin LiNick V. GrishinPublished in: Bioinform. (2013)
Keyphrases
- protein sequences
- genetic variation
- sequence data
- linkage disequilibrium
- single nucleotide polymorphisms
- human genome
- nucleotide sequences
- genome sequences
- high throughput
- computational approaches
- biological sequences
- sequence analysis
- complex diseases
- association studies
- genome wide
- computational biology
- genome wide association studies
- genomic data
- amino acids
- dna sequences
- protein structure prediction
- copy number
- protein structure
- secondary structure
- protein function
- haplotype inference
- protein classification
- multiple alignment
- protein secondary structure
- biological data
- protein structure and function