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- Software suite for analyzing DNA and protein sequence data from species and populations.3 KB (337 words) - 20:30, 15 December 2020
- ...population, as well as high coverage (i.e. greater than 30X) whole genome sequence data on a reference sample, or alternatively the availability of a set of r3 KB (344 words) - 13:45, 3 November 2020
- Computes a score between 0 and 100 for each site in the DNA sequence of a gene. A high score indicates an increased probability that n nucleotid3 KB (344 words) - 18:35, 10 June 2022
- than single sequence secondary structure prediction. Finally, RNAstructure3 KB (359 words) - 21:58, 21 August 2022
- Ensembl Tools provide a number of ready-made tools for processing sequence data.3 KB (333 words) - 18:52, 12 August 2022
- ...mer/read-based assembler that capitalizes on the high accuracy of Illumina sequence by eschewing an explicit error correction step which we argue to be redunda3 KB (354 words) - 18:36, 10 June 2022
- ...enced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt/Uniref90), protein domain identification (HMMER/PFAM3 KB (344 words) - 20:29, 7 December 2023
- reeTime provides routines for ancestral sequence reconstruction and inference of molecular-clock phylogenies, i.e., a tree w3 KB (370 words) - 17:44, 2 November 2020
- ...draft assembly by concatenating different parts of raw reads. This coarse sequence is then polished into a high quality assembly.3 KB (354 words) - 20:09, 24 August 2022
- ...nation of Minimizers and MinHash. This is then converted to an estimate of sequence identity using the Mash distance. An appropriate k-mer sampling rate is aut3 KB (359 words) - 17:28, 27 May 2022
- Robertson, James et al. “Universal whole-sequence-based plasmid typing and its utility to prediction of host range and epidem3 KB (340 words) - 20:03, 10 October 2022
- ...to generate indel calling, and then creates consensus sequences for indel sequence prediction.3 KB (351 words) - 15:41, 16 March 2023
- ...nce Alignment/Map) format is a generic format for storing large nucleotide sequence alignments. SAM is described in the SAMtools project page.6 KB (882 words) - 15:25, 27 January 2023
- MLST (multi-locus sequence typing) is a classic technique for genotyping bacteria, widely applied for3 KB (368 words) - 18:51, 10 June 2022
- AdapterRemoval may be used to recover a consensus adapter sequence for3 KB (357 words) - 20:47, 11 August 2022
- ...sta format. Briefly, it works in two step: first, BinPacker partitions the sequence data into many individual splicing graphs, each capturing the full transcri3 KB (365 words) - 12:53, 15 August 2022
- faSplit sequence ../large.fasta 120 blast_query_2 KB (358 words) - 20:27, 3 June 2022
- ...: " Musket: a multistage k-mer spectrum based error corrector for Illumina sequence data". Bioinformatics, 2013, 29(3): 308-315]3 KB (351 words) - 13:44, 19 August 2022
- ...for the creation and validation of whole genome and core genome MultiLocus Sequence Typing (wg/cgMLST) schemas, providing an allele calling algorithm based on3 KB (346 words) - 15:58, 20 October 2023
- analyses and also projected into coding sequence alignments for codon-based3 KB (375 words) - 18:17, 3 June 2022
- ...ng an iterative approach. In each iteration, it first estimates a multiple sequence alignment using the current tree as a guide and then estimates a ML tree on3 KB (381 words) - 19:31, 24 August 2022
- Bioinformatic sequence recovery for universal target-capture bait kits can be substantially improv3 KB (379 words) - 20:06, 12 August 2022
- ...tigs are provided as guidance to discovery novel viruses which do not show sequence similarity with known viruses.3 KB (377 words) - 23:22, 30 July 2020
- A minimum length open reading frame (ORF) is found in a transcript sequence3 KB (371 words) - 16:54, 22 August 2022
- the XML belonging to each sequence (provided in FASTA format). The program query sequence. Additionally you can add domain/motif based GO term obtained6 KB (920 words) - 14:08, 16 March 2023
- * aTRAM.pl: this script runs aTRAM with a target sequence and the formatted short-read archive.3 KB (350 words) - 15:23, 12 August 2022
- [https://arxiv.org/abs/1111.5572 Faster and More Accurate Sequence Alignment with SNAP. Matei Zaharia, William J. Bolosky, Kristal Curtis, Arm3 KB (372 words) - 20:42, 12 August 2022
- ...putative long non-coding RNAs by using an heuristic based on homology and sequence features.3 KB (387 words) - 21:18, 6 December 2019
- ...ool to perform guilt-by-contig-association classification of viral genomic sequence data. It's designed to cluster and provide taxonomic context of viral metag3 KB (358 words) - 20:04, 27 May 2022
- ...the Kraken database itself to derive probabilities that describe how much sequence from each genome is identical to other genomes in the database, and combine3 KB (402 words) - 19:01, 10 June 2022
- ...a Distributed Annotation Working Group (DAWG) in the annotation of genomic sequence contigs. These programs generate the multiple tracks of annotation evidence3 KB (381 words) - 21:20, 6 December 2019
- ...ttern search algorithm to rapidly select reads that contain an expected DR sequence. It then proceeds through reads identified in the previous step to find DR3 KB (392 words) - 17:58, 27 May 2022
- The reference sequence(s) can be whole genomes with multiple chromosomes, the transcriptome or eve3 KB (396 words) - 17:40, 21 August 2022
- ...which we term an Interpolated Context Model or ICM). The models for coding sequence are 3-periodic nonhomogenous Markov models. Improvements made in version 33 KB (391 words) - 17:09, 15 August 2022
- ...ational tool for identification of reassortments in influenza viruses from sequence databases of isolates. Reassortments in influenza - a process where strains3 KB (382 words) - 21:12, 7 December 2022
- 3) Reports various mitochondrial genes and sequence information in a simple table format.3 KB (382 words) - 14:27, 23 April 2020
- ...om raw reads or from assembled sequences, without the need for a reference sequence or de novo assemblies. SaffronTree takes FASTQ/FASTA files as input and use3 KB (400 words) - 17:17, 31 May 2022
- vcflib provides methods to manipulate and interpret sequence variation as it can be described by VCF. It is both:3 KB (390 words) - 20:54, 12 August 2022
- ...es. For each gene, Liftoff finds the alignments of the exons that maximize sequence identity while preserving the transcript and gene structure. If two genes i3 KB (399 words) - 13:14, 23 September 2020
- HaMSTR is a Hidden Markov Model based search tool to screen EST sequence data for the presence of putative orthologs to a pre-defined set of genes.3 KB (420 words) - 20:09, 12 August 2022
- ...es. antiSMASH not only detects the gene clusters, but also offers detailed sequence analysis.3 KB (409 words) - 21:11, 6 December 2019
- ...tao Yu, Changhai Zhang, Yuanning Liu, RunSheng Chen and Yi Zhao* Utilizing sequence intrinsic composition to classify protein-coding and long non-coding transc3 KB (374 words) - 14:09, 23 April 2021
- ...mic Poisson distribution to effectively capture local biases in the genome sequence, allowing for more sensitive and robust prediction. MACS compares favorably3 KB (384 words) - 19:47, 12 August 2022
- ...rms phylogenetic inference using the maximum-likelihood criterion. Several sequence types are supported, including nucleotide, amino acid and codon. Version 2.3 KB (485 words) - 16:53, 15 August 2022
- ...between sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. BLAST can3 KB (402 words) - 18:17, 12 August 2022
- ...to call variants in genetically heterogeneous populations from ultra-deep sequence data. It combines information regarding the covariation (i.e. phasing) betw3 KB (390 words) - 20:07, 27 May 2022
- sequence data generated with the PacBio No-Amp Targeted Sequencing4 KB (430 words) - 16:55, 15 December 2022
- ...n acyclic graph structure (a "pangenome reference"), which high-throughput sequence reads are re-aligned to for the purpose of discovering and genotyping SNPs,3 KB (373 words) - 15:43, 17 November 2021
- simultaneously on a sequence alignment, a matrix of quantitative characters3 KB (399 words) - 18:37, 12 August 2022
- * Simulated sequence evolution under specified scenarios of convergent evolution3 KB (380 words) - 22:12, 26 July 2023
- ...w-software-for-selection-of-phylogenetic-informative-regions-from-multiple-sequence-alignments/}} ...Gathering with Entropy), that is designed to select regions in a multiple sequence alignment that are suited for phylogenetic inference. For each character, B3 KB (407 words) - 13:04, 15 August 2022
- ...lter the connections by searching the merged gene sequences against public sequence databases. Finally, Rascaf uses these connections to select and/or re-arran3 KB (415 words) - 21:30, 21 August 2022
- ...ogram included with the system. If the species are too divergent for a DNA sequence alignment to detect similarity, then the PROmer program can generate alignm3 KB (393 words) - 13:39, 19 August 2022
- * Sequence Models3 KB (463 words) - 21:43, 7 November 2022
- ...eed of about 30 kb/second. It was implemented for large-scale human genome sequence analysis, but is applicable to other DNAs as well. It applies our COVE soft3 KB (389 words) - 20:53, 12 August 2022
- ...ly developed algorithm, Virus intEgration site detection through Reference SEquence customization (VERSE) (manuscript in consideration) as well as other new fe3 KB (410 words) - 21:29, 6 December 2019
- trimmer for Illumina Sequence Data. Bioinformatics.4 KB (452 words) - 18:44, 15 August 2022
- ...ources. It employs algorithmic techniques that scale well in the amount of sequence being aligned. For example, a pair of Y. pestis genomes can be aligned in u3 KB (448 words) - 19:49, 12 August 2022
- ...es to assemble discreet 'targets' contained within next-generation shotgun sequence data. ARC decomplexifies the traditionally difficult problem of assembly by3 KB (430 words) - 14:32, 12 August 2022
- ...ity of a virus population within a single host, it might be appropriate to sequence the pooled nucleic acid content of the virus in a blood sample from that ho3 KB (423 words) - 18:41, 1 June 2022
- BAli-Phy can estimate phylogenetic trees from sequence data when the alignment is uncertain. Instead of conditioning on a single a3 KB (402 words) - 17:19, 14 December 2022
- ...ordinates in a BAM file as if it had been built from a different reference sequence3 KB (456 words) - 18:00, 12 August 2022
- ...acterial plasmid contigs in short-read draft assemblies exploiting protein sequence-based replicon distribution scores. Microbial Genomics, 95, 295. https://do4 KB (437 words) - 17:14, 14 December 2022
- ...e of each base. These quality scores are used as the standard of consensus sequence calling. Combined with the prior probability of dbSNP allele, it gets a low3 KB (459 words) - 17:27, 15 August 2022
- Sequence assembler for very short reads.4 KB (523 words) - 17:06, 14 December 2022
- :: Scans a sequence file for adapters, and, based on a log-scaled threshold, determines a set o4 KB (438 words) - 14:54, 15 August 2022
- ...her classes of genes using protein annotations and/or assembled nucleotide sequence. AMRFinderPlus is used in the Pathogen Detection pipeline, and these data a4 KB (447 words) - 15:59, 27 May 2022
- kmerfreq count K-mer (with size K) frequency from the input sequence data,typically sequencing reads data, and reference genome data is also app3 KB (449 words) - 19:28, 12 August 2022
- ...strings there for the 3'-end cut. However, if the length of the remaining sequence is less than the minimum length threshold, then the read is discarded entir4 KB (551 words) - 22:56, 21 August 2022
- ...s by other bioinformatics software to accomplish this task have often used sequence alignment or machine learning techniques that were quite slow, leading to t4 KB (483 words) - 19:28, 12 August 2022
- ...s developed for the purpose of building genetic maps from RAD-Tag Illumina sequence data, but can also be readily applied to population studies, and phylogeogr4 KB (658 words) - 21:20, 2 January 2023
- ...entially to process large volumes of RNA-seq reads. Trinity partitions the sequence data into many individual de Bruijn graphs, each representing the transcrip4 KB (556 words) - 17:10, 22 August 2022
- ...two packages. Our SNP calling pipeline (Q score recalibration -> multiple sequence realignment -> snp/index calling) is a particular area of focus, and have b4 KB (540 words) - 16:53, 15 August 2022
- : Crusoe et al., The khmer software package: enabling efficient sequence analysis. 2014. doi: 10.6084/m9.figshare.9791904 KB (504 words) - 17:01, 14 December 2022
- * Other functionalities: Retrieve the nucleotide sequence in any user-specific genomic positions in batch, identify a candidate gene4 KB (545 words) - 14:16, 12 August 2022
- ...u were going to submit it to the queue. Be sure that you add the following sequence before the <code>mpiexec</code> command in your script:5 KB (754 words) - 19:24, 30 October 2023
- To transfer from a remote site to UFRC reverse the sequence in scenarios 2 and 3.10 KB (1,541 words) - 20:03, 17 January 2023