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資源導航

  • 資源導航
  • Personal genomics
1. CloudBurst
CloudBurst is a parallel read-mapping algorithm optimized for mapping next-generation sequence data to the human genome and other reference genomes.
標簽：SNP discovery,?Genotyping,Personal genomics
2. CopySeq
CopySeq analyzes the depth-of-coverage of whole genome resequencing data to predict CNVs and to infer quantitative locus copy-number genotypes.
標簽：Structural variation,?Copy number estimation,?Genotyping,Personal genomics
3. BRCA-diagnostic
Computational screening test for BRCA1/2 mutants in human genomic DNA
標簽：Personal genomics
4. GenomeJack
GenomeJack is a genome browser specialized in next-generation sequencing data. Advantages are intuitive interface and smooth drag'n drop response.
標簽：Genomics,?Personal genomics
5. MrCaNaVaR
mrCaNaVaR is a copy number caller that analyzes the next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.
標簽：Genomics,?Personal genomics,Copy number estimation
6. Ngs-pipeline
Complete solution for human re-sequencing projects
標簽：Personal genomics,Epigenomics,?Structural variation
7. SequenceVariantAnalyzer
DNA sequence information underpins genetic research, enabling discoversies of important biological or medical benefit. Compared with previous discovery strategies, a whole-genome sequencing study is no longer constrained by differing patterns of linkage disequilibrium, thus, in theory, ...
標簽：Personal genomics,?Genomics,Sequence analysis
8. Syapse
Syapse is a platform and application suite for bringing together omics and clinical data.
標簽：Allele-specific transcription,DNA methylation,?DNA-Seq,InDel discovery,?SNP discovery,?Structural variation,?RNA-Seq,?Small RNA transcriptome,?ChIP-Seq,Comparative genomics,Comparative transcriptomics,Epigenomics,?Genomics,Personal genomics,?Population ge