annotate_sv_type | Get SV type from svaba generated VCF |
bgzip | Bzips a VCF file |
call_ASEQ | Wrapper around ASEQ tool for pileup data. |
call_bcftools_parallel | Variant calling using bcftools on parallel per genomic region |
call_clonet | This function is a wrapper around CLONET function |
call_fings | Filters SNVs from any variant caller to remove false... |
call_fings_parallel | Filters SNVs from any variant caller to remove false... |
call_HaplotypeCaller | Wrapper for GATK HaplotypeCaller for Germline Variant calling |
call_mutect2 | Variant calling using MuTECT2 |
call_mutect2_parallel | Variant calling using MuTECT2 on parallel per genomic region |
call_platypus | Variant calling using Platypus |
call_segments | Call segments for panel, exome and WGS data using CNVkit This... |
call_sv_manta | Call Somatic/Germline structural variants using Manta This... |
call_sv_manta_parallel | Call Somatic/Germline variants using MANTA in parallel This... |
call_sv_svaba | Structural variant calling using svaba |
call_sv_svaba_parallel | Structural variant calling using svaba in parallel |
call_variants | Variant calling of Somatic and Germline (MuTECT2, Platypus... |
call_variants_strelka | Call Somatic/Germline single nucleotide variants using... |
call_variants_strelka_parallel | Call Somatic/Germline variants using Strelka in parallel This... |
call_vep | Predict variant effect using VEP |
call_vep_maf | Variant annotation in MAF format |
check_and_unzip | Check and unzip gz compressed file |
CNNScoreVariants | Annotate a VCF with scores from a Convolutional Neural... |
compress_and_index_vcf | Compress and index vcf file |
estimate_contamination | VCF contamination estimation using GATK |
estimate_contamination_parallel | VCF contamination estimation using GATK |
FilterVariantTranches | Filter Variant Tranches (Mutect2) |
filter_VEP | Filter VEP results |
fix_mnps | VCF fix MNPs |
format_ASEQ_pileup | ASEQ pileup formatting for downstream analysis This function... |
format_PM_data | Format vcf for downstream point mutatation analysis. |
format_segment_data | Format segmentation data for downstream analysis using... |
format_SNP_data | This function filter and formats heterozygous SNP data for... |
generate_CLONET_config | This function generates a config files for CLONET pipeline |
generate_CLONET_sample_info | This function generates a sample_info file for CLONET... |
generate_sets | Generate a 1:n sets between a group of vcfs |
get_pileup_summary | BAM pileup summary for known sites using GATK |
get_sv_type | Get SV type from svaba generated VCF |
learn_orientation | Learn Read Orientation Model (Mutect2) |
merge_maf | This function merges a group of files in MAF format This... |
pipe | Pipe operator |
plot_allelic_imbalance | This function generates a plot of allelic imbalance from... |
plot_celullarity | This function generates a plot of ploidy and celularity... |
plot_cn_calls | This function generates a plot of ploidy and celularity... |
plot_evolutionary_distance | This function generates a plot of reltionship between samples... |
process_maf | This function processes a MAF file This function takes the... |
process_variants | Process variants generated using variant_call and... |
split_vcf | Splits multisample VCF file into multiple VCFs |
tab_indx | Index tab separated genomic regions |
vcf_annotate | VCF annotation using bcftools |
vcf_bcftools | Variant calling using bcftools |
vcf_communality | VCF communality |
vcf_concatenate | VCF file concatenation |
vcf_filtering | VCF filtering using GATK |
vcf_filter_variants | VCF filtering using bcftools |
vcf_format | VCF formating using bcftools |
vcf_intersect_bed | Intersect vcf with bed file |
vcf_sets | Generate a set between a group of vcfs usign bcftools |
vcf_sort | Sort VCF file |
vcf_stats_merge | VCF stats file concatenation |
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