WebDec 6, 2024 · BD Rhapsody pipeline for whole transcriptome analysis was used to identify the molecular index sequences (position 49-56) and align reads to predfined cell label sequences (position 1-8,22-30,43-51) on Read1, and to align reads (Read2) to the human transcriptome (hg19, gencode annotation) using STAR with default parameters. ... The BD Rhapsody™ Single-Cell Analysis System provides reliable and reproducible results making it an ideal system for translational studies. The system offers superior cell capture rates and low multiplet rates with a variety of cell types as compared to other systems.
Workflow: BD Rhapsody™ Targeted Analysis Pipeline
WebA wrapper for the BD Rhapsody Analysis CWL v1.10.1 pipeline Bbknn: Neighbors BBKNN network generation Bcl convert: Demux Convert bcl files to fastq files using bcl-convert. Bcl2fastq: Demux Convert bcl files to fastq files using bcl2fastq Build bdrhap reference: Reference Compile a reference into a STAR index compatible with the BD Rhapsody ... Webv1.9.1 of the BD Rhapsody™ Analysis Pipeline for improved WTA Analysis Released: Improved putative cell calling algorithm to reduce overcalling of putative cells in high … canadian jet stream map
BD Rhapsody™ Single-Cell Analysis System - BD …
Webv1.9.1 BD Rhapsody Analysis Pipeline for improved WTA Analysis Released. Slide deck: BD Rhapsody™ Single-Cell Analysis System: A robust microwell-based single-cell partitioning system for high-dimensional biology research (Sept 2024) Protocol: BD Rhapsody™ high-plex AbSeq (up to 100 plex)+SMK protocol (May 2024) Slide deck: … WebMar 16, 2024 · Velocyto.py for BD Rhapsody. This is a minimal nextflow workflow to run velocyto.py on BAM files produces by the BD Rhapsody pipeline. It consists of two steps: manipulating the BAM file to make it compatible with velocyto. running velocyto.py. WebSep 18, 2024 · In the “Apps” section of the project, click on “add app” and select the “BD Rhapsody™ Targeted Analysis Pipeline” by clicking “run. 43. In the new screen, navigate to the “Inputs” section on the left hand side, select the AbSeq .fasta file as the “AbSeq Reference”, the .fastq files for the “Reads”, and the mRNA ... canadian knock knock jokes