Index of /public/dataset/MAS-Seq-bulk

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INTRODUCTION
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Last Updated: 06/01/2023

This README file describes the contents in this directory.

This is a preliminary data release of MAS-Seq for Bulk Iso-Seq kit. Data is subject 
to modification until the final release.



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SAMPLE
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Revio-HG002-1
Vendor – Coriell
Lot No – n/a
HG002 cells were purchased from Coriell and grown in RPMI1640 w/Glutamax media with 
16% FBS and 0.5% Penicillin-Streptomycin. RNA was isolated from 10x10^6 HG002 cells 
using Trizol reagent and Phasemaker tubes. RNA quality was assessed using a Bioanalyzer.



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METHODS
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Library Preparation: 
(Unreleased) Procedure & Checklist - Preparing MAS-Seq libraries using MAS-Seq for bulk Iso-Seq kit

Sequencing: 
Revio system with Revio polymerase kit and Revio sequencing plate

Run time: 
Revio – 24 hr movie

Analysis: 
(Unreleased) Read segmentation and Iso-Seq workflow

   
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FILE DESCRIPTION
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Each sample will contain the following folders:


========================
1-Sreads
========================

This directory contains segmented reads that have been processed by Read segmentation (or skera) [1]
to produce S-reads that represent the original cDNA molecules. segmented.bam contains S-reads that 
have the expected order of MAS adapters and is the file used in carrying the subsequent analyses.

1-Sreads/
├── segmented.bam
└── segmented.non_passing.bam


========================
2-FLNC
========================

This directory contains full-length, non-concatemer (FLNC) reads that have been removed of the 
5' and 3' cDNA primer as well as the polyA tail. FLNC reads are oriented from 5'->3' based on 
the asymmetry of the cDNA primers.


2-FLNC/
└── flnc.bam


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3-ClusterMap
========================

This directory contains HQ cluster sequences by clustering FLNC reads at the isoform level de novo. 
The HQ cluster reads are then mapped using pbmm2 (minimap2 wrapper) to hg38.

3-ClusterMap
├── clustered.bam
└── mapped.bam


========================
4-Collapse
========================

This directory contains the result of collapsing redundant isoforms after HQ cluster sequences were 
mapped to the genome. Each collapsed isoform has an unique ID `PB.X.Y` with an associated FLNC read count.

4-Collapse
├── collapsed_transcripts.fasta 
├── collapsed_transcripts.flnc_count.txt 
├── collapsed_transcripts.gff 
├── collapsed_transcripts.group.txt
└── collapsed_transcripts.read_stat.txt 


========================
5-Pigeon
========================


This directory lists the the total set of unique transcripts as a result of mapping the dedup reads 
to the genome, collapsed into transcripts, classified and filtered against Gencode using pigeon. 
Read about pigeon at [2]. 

The classification.txt and junctions.txt are the output from pigeon showing the per-isoform and 
per-junction-per-isoform classification results against Gencode annotation. The GFF3 file shows 
the exonic structures of the transcript isoforms. 


5-Pigeon/
├── pigeon_classification.filtered_lite_classification.txt 
├── pigeon_classification.filtered_lite_junctions.txt 
├── pigeon.sorted.filtered_lite.gff 
└── pigeon_classification.filtered_lite_pigeon_report.pdf



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REFERENCES
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[1] skera.how https://skera.how/

[2] isoseq.how https://isoseq.how/




Research use only. Not for use in diagnostic procedures.
 © 2023 Pacific Biosciences of California, Inc. (“PacBio”). All rights reserved. 
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