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Status |
Public on Oct 04, 2022 |
Title |
Soy Leaf 40ng Rep 1 |
Sample type |
SRA |
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Source name |
Soy leaf
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Organism |
Glycine max |
Characteristics |
strain: Wm82 technique: smar2C2 tissue: Leaf
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Growth protocol |
Plants grown for four weeks with standard 16H daylight conditions at room temperature
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Extracted molecule |
polyA RNA |
Extraction protocol |
RNA was extracted using Monarch Total RNA Extraction and Purification kit (NEB #T2010) Libraries where prepared using the novel smar2C2 method described in the related manuscript
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
Sequences were quality trimmed and adaptors were identified and filtered using CutAdapt v2.8 UMI sequences were extracted from processed fasta files using UMI-tools v1.0.1 Sequences were aligned to their respective genome using STAR v2.7.2 Sequences were deduplicated using the UMI and mapping location using UMI-tools v1.0.1 Transcriptoinal start sites were determined using the R library TSRchitect v1.2.0 in R v4.0.0 Genome_build: Maize genome = AGPv4.38, Sorghum genome = NCBIv3.52, Rice genome = IRGSP-1.0.51, Wheat genome = IWGSC.51, Soy genome = Wm82.a4.v1 Supplementary_files_format_and_content: Text file containing single nucleotide position of transcription start site, read count, and strand
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Submission date |
Feb 22, 2022 |
Last update date |
Oct 04, 2022 |
Contact name |
Robert J Schmitz |
E-mail(s) |
[email protected]
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Organization name |
University of Georgia
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Department |
Genetics
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Street address |
B416 Davison Life Sciences
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City |
Athens |
State/province |
GA |
ZIP/Postal code |
30602 |
Country |
USA |
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Platform ID |
GPL28801 |
Series (1) |
GSE197144 |
Simple and Accurate Transcriptional Start Site Identification Using Smar2C2 |
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Relations |
BioSample |
SAMN26156426 |
SRA |
SRX14249627 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data not provided for this record |
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