WebMar 14, 2024 · Tracy can be easily integrated in large-scale pipelines and high-throughput settings, and it uses state-of-the-art file formats such as JSON and BCF for reporting chromatogram sequencing results and variant calls. Webbamsnap bcftools bedops bedtools bioconda bowtie2 bwa bwa-mem2 cufflinks cnvkit cnvnator cutadapt delly dicey elprep fastp fastq-dump fastqc fgbio freec gatk gencore gffread gridss goleft hisat2 igv igv-webapp jbrowse kallisto last lumpy macs2 manta miso msisensor msisensor-pro multiqc nirvana oncotator picard pindel prinseq rsem …
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WebAug 7, 2024 · The analysis and interpretation of datasets generated through sequencing large numbers of individual genomes is becoming commonplace in population and … WebGEAR: genome analysis server genome analysis server alfred AL BAM file statistics. ancient AN Ancestry inference with convolutional neural networks. bgen BG Heuristic … Application Description. Teal is a tool to view sanger trace files and extract the … Application Description. Indigo is a rapid SNV and InDel discovery method for … Application Description. Pearl is a tool to patch a DNA references with several … Application Description. Sage is a tool to view sanger trace files aligned to a … Generate dissimilar barcode sequences with balanced, per-position base … Application Description. Salt is a tool to align a reference (target sequence) to a … Browse haplotype-resolved data, e.g. from Strand-seq experiments. Application Description. Silica runs a virtual insilico PCR with a set of primers on a … intrepiddg.com
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WebApr 7, 2024 · Here, we provide a computational workflow for predicting anchor locations for a wide range of HLA alleles using a seed dataset generated from a collection of patient samples from local tumor sequence studies ( 30) combined with samples from the Cancer Genome Atlas (TCGA). WebJan 11, 2024 · Berry Genomics is dedicated to research, development and commercialization of genetic test technologies in clinical applications. Berry Genomics … WebOct 29, 2024 · indigo - gear-genomics :ゲノムリファレンスを選択して解析できる。シーケンスデータがリファレンス配列と合致する領域であるか確信をもてない場合は有用かもしれない。論文は未発表、emblがサ … newmen through axle