|
Status |
Public on May 22, 2018 |
Title |
mRNA Medicago HM108 |
Sample type |
SRA |
|
|
Source name |
plant
|
Organism |
Medicago truncatula |
Characteristics |
ecotype: HM108 tissue: mature leaves age: 45 days
|
Treatment protocol |
the plant was grown in the greenhouse under long day conditions during the winter
|
Extracted molecule |
total RNA |
Extraction protocol |
MethylC-seq libraries were prepared as previously described in (Urich et al. 2015). RNA-seq libraries were constructed using Illumina TruSeq Stranded RNA LT Kit (Illumina, San Diego, CA) following the manufacturer’s instructions with limited modifications. The starting quantity of total RNA was adjusted to 1.3 μg, and all volumes were reduced to a third of the described quantity. Small RNA-seq libraries were prepared using the Illumina TruSeq Small RNA Library PrepKit v2 according to the manufacturer's instructions.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
MethylC-seq: MethylC-seq analysis was performed as described in (Schmtiz et al. 2013) RNA-seq: RNA-seq was performed using TopHat v2.0.13 and Cufflinks v2.2.1 small RNAseq was performed using Illumina small RNA TruSeq library prep kit,and using bowtie for sequence mapping Genome_build: Mtruncatula_285_Mt4.0 Supplementary_files_format_and_content: tab delimited text file, see "allc_header_descriptions.txt", "smallRNA.processedfile_description.txt" and "RNA_column_header_descriptions.txt" for column headers
|
|
|
Submission date |
May 21, 2018 |
Last update date |
May 22, 2018 |
Contact name |
Robert J Schmitz |
E-mail(s) |
[email protected]
|
Organization name |
University of Georgia
|
Department |
Genetics
|
Street address |
B416 Davison Life Sciences
|
City |
Athens |
State/province |
GA |
ZIP/Postal code |
30602 |
Country |
USA |
|
|
Platform ID |
GPL17491 |
Series (1) |
|
Relations |
BioSample |
SAMN09233952 |
SRA |
SRX4109198 |