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- Short read RNASeq de novo assembly is a well established method to study transcription of organisms lacking a2 KB (280 words) - 21:20, 6 December 2019
- ...uses SPAdes at its core, but alters the steps before and after the primary assembly step to get similar results in less time. Shovill also supports other assem2 KB (286 words) - 18:13, 23 August 2022
- # The length cutoff used for seed reads usef for pre-assembly2 KB (248 words) - 20:31, 2 August 2021
- ...es from such complex datasets, and it is also being applied to the de novo assembly of large individual genomes.2 KB (286 words) - 16:26, 10 June 2022
- ...eline for identifying large-scale structural variants, performing sequence assembly at the breakpoints, and reconstructing the complex structural variants usin2 KB (274 words) - 21:21, 6 December 2019
- ...KB Seah, Elmar Pruesse. phyloFlash — Rapid SSU rRNA profiling and targeted assembly from metagenomes.]2 KB (279 words) - 00:09, 29 October 2020
- ...arisons between a large number of genomes, with a focus on handling genome assembly data.2 KB (278 words) - 16:25, 10 June 2022
- A tool to order and orient genome assembly contigs via Minimap2 alignments to a reference genome.2 KB (280 words) - 21:24, 6 December 2019
- ...Li. 2018. GetOrganelle: a fast and versatile toolkit for accurate de novo assembly of organelle genomes. bioRxiv, 256479.]2 KB (275 words) - 21:21, 6 December 2019
- # The length cutoff used for seed reads usef for pre-assembly2 KB (266 words) - 20:30, 2 August 2021
- ...allows a user to bypass several standard steps, including read filtering, assembly, gene prediction, gene annotation, all vs. all comparisons, orthology predi2 KB (292 words) - 18:42, 12 July 2023
- ...ritz, A., Bremges, A., Deng, ZL. et al. Haploflow: strain-resolved de novo assembly of viral genomes. Genome Biol 22, 212 (2021)]2 KB (287 words) - 20:31, 3 January 2022
- [[Category:Assembly]]2 KB (295 words) - 17:31, 15 August 2022
- [[Category:Software]][[Category:Biology]][[Category:Assembly]]3 KB (300 words) - 14:02, 15 August 2022
- ...works applied from a pileup of individual sequencing reads against a draft assembly. It outperforms graph-based methods operating on basecalled data, and can b2 KB (290 words) - 14:37, 21 August 2023
- ...s in FastQ format. Mapping to a whole-genome reference sequence or de novo assembly or the short reads is not necessary.2 KB (287 words) - 15:26, 21 June 2023
- [[Category:Software]][[Category:assembly]]2 KB (284 words) - 21:14, 20 November 2023
- HapCompass implements a novel HAPCOMPASS algorithm for haplotype assembly of densely sequenced human genome data. The algorithm operates on a graph w2 KB (287 words) - 18:13, 15 August 2022
- ...e novo assembler for PacBio and Oxford Nanopore (ONT) data. It produces an assembly from all-vs-all raw read alignments without an error correction stage. It a2 KB (296 words) - 21:24, 6 December 2019
- ...gnificantly improve genome assemblies. They can also improve transcriptome assembly when FLASH is used to merge RNA-seq data.2 KB (297 words) - 16:44, 15 August 2022
- ...290925 Dierckxsens N., Mardulyn P. and Smits G. (2016) NOVOPlasty: De novo assembly of organelle genomes from whole genome data. Nucleic Acids Research, doi: 13 KB (310 words) - 21:23, 6 December 2019
- ...sequencing reads. stringMLST predicts the ST of an isolate in a completely assembly and alignment free manner. The tool is designed in a light-weight, platform2 KB (292 words) - 20:45, 12 August 2022
- |{{#vardefine:url|https://support.10xgenomics.com/de-novo-assembly/software/}} Supernova is a software package for de novo assembly from Chromium Linked-Reads that are made from a single whole-genome library3 KB (306 words) - 16:55, 10 June 2022
- ...ces a new graph binning algorithm and achieves the best haplotype-resolved assembly given trio data.3 KB (303 words) - 22:23, 27 August 2020
- ...ific use cases: 1) to robustly estimate the base accuracy of CCS reads and assembly contigs, and 2) to investigate the systematic error rate of CCS reads. It a2 KB (293 words) - 16:10, 10 March 2021
- Multi-sample de novo assembly and variant calling using Linked de bruijn graphs. Variant calling with and3 KB (297 words) - 22:22, 8 September 2020
- ...are generated independently when all binning tools are applied to the same assembly.3 KB (315 words) - 21:21, 6 December 2019
- YASRA (Yet Another Short Read Assembler) performs comparative assembly of short reads using a reference genome, which can differ substantially fro3 KB (304 words) - 20:56, 12 August 2022
- ...ise, which is presented as low-quality bases, has serious impact on genome assembly and mapping. We propose SeqyClean, a specialized cleaning pipeline that all3 KB (312 words) - 22:41, 21 August 2022
- ...assemblies for the same isolate, Trycycler can combine them into a single assembly that is better than any of your inputs.3 KB (305 words) - 18:13, 22 July 2021
- ...s without error correction and then builds the consensus from intermediate assembly output. Wtdbg2 is able to assemble the human and even the 32Gb Axolotl geno3 KB (310 words) - 17:44, 22 August 2022
- title={Recycler: an algorithm for detecting plasmids from de novo assembly graphs},3 KB (297 words) - 14:21, 11 October 2022
- ...rom minimap2) and detects five different variant classes between the query assembly and the reference: deletions, insertions, tandem and interspersed duplicati3 KB (306 words) - 17:16, 31 May 2022
- Corset is a command-line program to go from a de novo transcriptome assembly to gene-level counts. Our software takes a set of reads that have been mult3 KB (309 words) - 17:09, 10 June 2022
- ...t requires a set of target transcripts (either from a reference or de-novo assembly) to quantify. All you need to run Salmon is a FASTA file containing your re3 KB (305 words) - 19:29, 3 June 2022
- [[Category:Software]][[Category:Biology]][[Category:Genomics]][[Category:Assembly]]2 KB (313 words) - 20:42, 18 August 2022
- HASLR is a tool for rapid genome assembly of long sequencing reads. HASLR is a hybrid tool which means it requires lo3 KB (315 words) - 19:53, 17 August 2020
- ...l-vs-all read self-mappings (typically by minimap) as input and outputs an assembly graph in the GFA format. Different from mainstream assemblers, miniasm does3 KB (306 words) - 20:10, 18 August 2022
- [[Category:Software]][[Category:Biology]][[Category:Assembly]][[Category:Genomics]]2 KB (297 words) - 19:41, 21 August 2022
- ...create a new processed sequence file as output. This design encourages the assembly of the seq_crumbs utilities with Unix pipes to create complex pipelines. Th3 KB (328 words) - 15:12, 27 May 2022
- ...peats directly from sequence reads. It based on the idea of frequent k-mer assembly. REPdenovo provides many functionalities, and can generate much longer repe3 KB (327 words) - 21:43, 21 August 2022
- ...), but requires significantly less computing resources and storages. After assembly, the per-base accuracy is about 98-99.8%, to further improve single base ac3 KB (312 words) - 18:03, 10 May 2021
- ntEdit is a scalable genomics application for polishing genome assembly drafts. ntEdit simplifies polishing and "haploidization" of gene and genome3 KB (316 words) - 21:23, 6 December 2019
- IVA: accurate de novo assembly of RNA virus genomes.2 KB (300 words) - 16:06, 7 December 2021
- ...r the representation of de Bruijn graphs are important for genome sequence assembly. A fully dynamic data structure supporting efficient and exact membership q3 KB (312 words) - 21:20, 6 December 2019
- ...ta, profiled from solid tissues, including tumors. TRUST4 performs de novo assembly on V, J, C genes including the hypervariable complementarity-determining re3 KB (314 words) - 20:12, 8 February 2021
- ...present in scaffold assemblies, especially those generated by the de novo assembly of whole genomes with next-generation sequencing (NGS) reads. Unlike other3 KB (321 words) - 17:25, 10 June 2022
- ...n Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement. PLoS ONE 9(11): e112963. doi:10.1371/journal.pone.0112963]3 KB (321 words) - 20:23, 12 August 2022
- ...zov YB, Campbell EM, Switzer WM, Skums P, Mangul S, Zelikovsky A. Accurate assembly of minority viral haplotypes from next-generation sequencing through effici3 KB (301 words) - 20:24, 1 May 2024
- ...ced with 'N' symbols. Occasionally, if the genome is in the early stage of assembly the non-masked sequences are too short for most reference indexes to be bui2 KB (361 words) - 20:30, 12 August 2022