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 … WebJul 19, 2024 · gear-genomics / bgen Star 2 Code Issues Pull requests Barcode Generator genomics dna high-throughput-sequencing dna-sequences dna-sequencing dna-barcode gear-genomics Updated on Jan 9 JavaScript rocamador / ftdna-matches Star 2 Code Issues Pull requests Retrieve FTDNA (Family Tree DNA) matches genealogy dna …
GEAR · GitHub
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. WebWelcome to our online catalog, SwitchDB! Search across our genome-wide collection of Assay-Ready Constructs for your promoter and UTR reporters New Users Register Now Search by gene, pathway, transcription factor motif or miRNA sequence Download a sales quote to order today timex snoopy watch vintage
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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). WebMar 14, 2024 · Tracy can be routinely applied in large-scale validation efforts conducted in clinical genomics studies as well as for high-throughput genome editing techniques that … WebIndigo is a rapid single-nucleotide variant (SNV) and insertion/deletion (InDel) discovery method in Chromatogram traces obtained from Sanger sequencing of PCR products. It can separate a mutated and wildtype allele and aligns both alleles against a reference sequence or wildtype chromatogram. Indigo discovers mutations generated by genome editing … parking at metra train stations