Kai Wang

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Circular RNAs are abundant, conserved, and associated with ALU repeats

The MicroRNA Spectrum in 12 Body Fluids

Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Hierarchical Nanocomposites of Polyaniline Nanowire Arrays on Graphene Oxide Sheets with Synergistic Effect for Energy Storage

MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery

Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies

Multiple early factors anticipate post-acute COVID-19 sequelae