Annotation

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Query returned 20 results.

  Biological domain Bioinformatics method Input format Output format
ANNOVAR Genomics
Genetics
Annotation
Variant prioritisation
BioNumerics Workflows
Comparative genomics
Quality control
Data handling
Sequence assembly
Epidemiology
Microbial Surveillance
Genotyping
Whole genome resequencing
Sequence analysis
Sequence assembly
Read mapping
Annotation
Variant calling
Comparative genomics
Workflows
Sequence alignment
Genome visualisation
.ab1
(C)FAST(A/Q)
.bam
FNAQual
Compressed fastq
And many others.
CLCbio Genomics Workbench Genomics
Whole genome resequencing
Sequence assembly (de novo assembly)
SNP detection
Indel detection
ChIP-seq
RNA-Seq
Regulatory RNA
Transcriptomics
Mapping
Read mapping
Sequence assembly
Sequence alignment
Ab-initio gene prediction
Adapter removal
Annotation
Bisulfite mapping
SNP calling
Sequence assembly (de-novo assembly)
Heat map generation
Sequence assembly validation
FASTA
FASTQ
GenBank
SAM
BAM
Illumina Bustard
ELAND
CSFASTA/CSQUAL (ABI SOLiD)
FASTA
FASTQ
GFF
GenBank
SAM
BAM
ACE
Nexus
CSV
PDF
XLS
CRAVAT Genomics
Genetics
Genetic variation
Annotation
Variant prioritisation
Sequence annotation
SNP annotation
Variant classification
VCF
TSV
TSV
Genedata Expressionist Genomics
Epigenetics
SNP detection
Indel detection
ChIP-seq
RNA-Seq
Transcriptomics
Sequencing
Copy number estimation
Gene structure
DNA methylation
Laboratory information management
Sequence alignment
Annotation
Bisulfite mapping
Clustering
Gene expression analysis
Genome visualisation
Read mapping
Sequencing quality control
RNA-Seq analysis
Sequence analysis
Statistical calculation
2bit
FASTA
Nib
FASTQ
QSEQ
BAM
SAM
BedGraph
VCF
BED
GDC
GFF
GTF
And many others.
Geneious Phylogenetics
Sequence analysis
Sequence assembly (de novo assembly)
Genomics
Population genetics
Metagenomics
Structural variation
RNA-Seq
Epigenomics
Sequence alignment
Sequence assembly
Sequence assembly validation
Annotation
Genome visualisation
DNA barcoding
Read mapping
Visualisation
Sequence motif discovery
Variant calling
FASTA
FASTQ
GenBank
SAM
ELAND
CSFASTA
CSQUAL
GeneTalk Structural variation Variant calling
Genetic variation analysis
Sequence contamination filtering
Annotation
Exome analysis
Sequence analysis
Variant classification
Plotting and rendering
VCF VCF
XLS
XLSX
Golden Helix Epigenomics
Genomics
Sequencing
SNP detection
Copy number estimation
Data handling
Sequencing quality control
Statistical calculation
Genome visualisation
Annotation
Sequence contamination filtering
Collapsing methods
Variant classification
Variant calling
KBASE Comparative genomics Annotation
Lasergene Sequence assembly (de novo assembly)
Genomics
Indel detection
Phylogenetics
Protein structure analysis
Mapping
SNP detection
Sequence analysis
Transcription factors and regulatory sites
Sequence alignment
Sequence alignment analysis
Annotation
Sequence assembly
Chromatogram visualisation
Sequence analysis
Read mapping
PCR primer design
Scaffolding
Peak calling
LSKB, Life Science Knowledge Bank Genomics Analysis pipeline
Annotation
SNP calling
Classification
Pathway or network analysis
Sequence analysis
Functional analysis
Differential expression analysis
MG-RAST Metagenomics
Phylogenetics
Metabolic reconstruction
Annotation FASTA
FASTQ
(Compressed) FASTA
(Compressed) FASTQ
SFF
BIOM
FASTA
NucleR ChIP-on-chip
ChIP-seq
DNA packaging
Epigenomics
Annotation
Peak calling
ShortRead
BioConductor
WIG
BED
BioConductor
Proxygenes Metagenomics Read mapping
Annotation
RAST Genomics
Phylogenetics
Annotation
Genomics
Segtor SNP Annotation
SNP annotation
Tab-delimited Tab-delimited
SeqBuster Transcriptomics
Regulatory RNA
Read mapping
Annotation
FASTA
Tab-delimited
Tab-delimited
SequenceVariantAnalyzer Personalised medicine
Genomics
Sequence analysis
Genetic variation
Annotation
Genome visualisation
SNP calling
SAMtools
HMMCNV
Sva
Vectorfriends Sequence alignment
Sequence assembly
Annotation
Sequence alignment visualisation
Visualisation
WebApollo Genomics
Sequence annotation
Sequence functional annotation
Annotation GFF3
BigWig
BAM
GFF3
BED
Personal tools
Namespaces

Variants
Actions
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Software
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