必应词典为您提供next-generation-sequence的释义,网络释义: 高通量测序;下一代测序;
Next-generation sequencing, in contrast, makes large-scale whole-genome sequencing (WGS) accessible and practical for the average researcher. It enables scientists to analyze the entire human genome in a single sequencing experiment, or sequence thousands to tens of thousands of genomes in one year...
Fast, flexible, and simple next-generation sequencing for forensics with the Ion GeneStudio S5 Systems Ion GeneStudio S5 System Ion GeneStudio S5 Plus System Ion GeneStudio Prime System Want to sequence SNP panels on Monday, mtDNA panels on Wednesday, and ...
The design of highly multiplex PCR primers to amplify and enrich many different DNA sequences is increasing in biomedical importance as new mutations and pathogens are identified. The authors present and experimentally validate Simulated Annealing Design using Dimer Likelihood Estimation (SADDLE), a stoc...
次世代定序 SLC22A12ABCG2Next generation sequenceSnapshot assay台灣目前痛風盛行率為全世界第一,且有逐漸年輕化的趨勢.已有研究指出在調節血液中尿酸濃度的SLC22A12及ABCG2上發現的SNPs與痛風都具有相關性,但在國內的相關資料還需釐清.利用次世代定序來分析正常,高尿酸血症及痛風族群各48,19及48支檢體.結果顯示...
In this Tools of the Trade article, Carly Tyer describes the development of Telo-seq, a method to enrich and sequence all telomeres within a sample, and highlights its use in distinguishing between the two telomere maintenance mechanisms used in cancer cells. Carly Tyer Research Highlights22 Oct...
Artemis is a free genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation bioinformatics research genomics pathogen sequencing next-generation-sequencing bioinformatics-pipeline global-...
Primary equipment already available in most labs. Next Generation Sequencing (NGS) Advantages High sample throughput High sensitivity Comprehensive genomic coverage Can sequence thousands of genes simultaneously Low sample input required Fast turnaround time for high sample volumes ...
Diagenode has specialized in epigenetics studies for over 15 years. We first developed a unique shearing system for chromatin for ChIP studies. Our expertise easily lent itself to state-of-the art shearing devices for DNA, now down to shearing volumes of 5 ul, perfect for NGS DNA library prep...
The transformation of raw sequence data into actionable information is complex and computationally intensive (Figure). The first step is typically to assemble shorter fragments into a complete sequence, either by mapping against a known reference genome or by assembling the sequence de novo using overl...