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Status |
Public on May 05, 2021 |
Title |
LoopSeq Synthetic Long Read Sequencing Uncovers Isoform Modulation in the progression of Colon Cancer [RNA-seq] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
In this study, we used a barcoding-based synthetic long read (SLR) isoform sequencing approach (LoopSeq) to generate sequencing reads sufficiently long and accurate to identify isoforms using standard short read Illumina sequencers.
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Overall design |
Amplicon RNA-sequencing targeting on gene FAM104A and PABPC1 across 6 colon cancer samples. ID 1, 2 and 3 are for patient ID. T and M are for tumor and metastasis samples. GRM and PHU are for two enzymes.
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Contributor(s) |
Liu S, Wu I, Yu Y, Balamotis M, Ren B, Yehezkel TB, Luo J |
Citation(s) |
33907296 |
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Submission date |
Jul 29, 2020 |
Last update date |
May 05, 2021 |
Contact name |
Shuchang Liu |
E-mail(s) |
[email protected]
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Organization name |
University of Pittsburgh
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Street address |
203 Lothrop Street
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City |
Pittsburgh |
State/province |
PA |
ZIP/Postal code |
15261 |
Country |
USA |
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Platforms (1) |
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Samples (16)
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This SubSeries is part of SuperSeries: |
GSE155921 |
LoopSeq Synthetic Long Read Sequencing Uncovers Isoform Modulation in the progression of Colon Cancer |
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Relations |
BioProject |
PRJNA656188 |
SRA |
SRP276916 |