Webb18 sep. 2024 · Depending on the selection of tools, the particular pipeline will run.Results: This tab enables users to visualize output statistics of the tools used, and the major output files, specifically, the variants called and the annotated variants in the case of DNA-Seq pipeline, and differentially expressed genes for RNA-Seq pipeline. http://ccb.jhu.edu/software/stringtie/index.shtml?t=manual
HISAT2-STRINGTIE-BALLGOWN pipeline · GitHub - Gist
WebbHISAT-3N Overview. HISAT-3N (hierarchical indexing for spliced alignment of transcripts - 3 nucleotides) is designed for nucleotide conversion sequencing technologies and implemented based on HISAT2. There are two strategies for HISAT-3N to align nucleotide conversion sequencing reads: standard mode and repeat mode.The standard mode … WebbI am using the Hisat2 - Stringtie - Ballgown pipeline that was published in nature protocols in 2016. When I upload my ballgown data in to r, I have 4 lane technical replicates per biological sample, in addition to 3 biological samples per condition (2 conditions total). This leads to 24 "samples" as Ballgown calls it. cea boushey
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WebbHave 16 samples run thru hisat2 with the --dta and stringtie with -B option, made pheno_data, and ballgown dir with the 16 sample dir with the .ctab and .gtf files for each sample. Got to run in ballgown ok, and made .csv files for genes and transcripts. What I need to do now is tell ballgown how to handle the 16 samples. Webb13 feb. 2024 · A front-end GUI to map NGS DNA sequencing data using HISAT backend tool. This software offers robust seamless queueing of the mapping operations along … WebbWhen running the HISAT2/StringTie/Ballgown pipeline, known gene/transcript annotations are used for several purposes: During the HISAT2 index creation step, annotations may be provided to create local indexes to represent transcripts as well as a global index for the entire reference genome. cea body