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ERX1460293

FASTQ

SRA

Experiment Detail

TitleIllumina HiSeq 2500 paired end sequencing; Distinct and sexually dimorphic X dosage compensation states in the mammalian germline
Design DescriptionDistinct and sexually dimorphic X dosage compensation states in the mammalian germline
OrganismMus musculus

Library Description

NameSample 184
StrategyRNA-Seq
SourceTRANSCRIPTOMIC
SelectionRT-PCR
LayoutPAIRED
Orientation
Nominal Length300
Nominal Sdev100
Construction ProtocolTimed matings were undertaken, and noon on the date of the vaginal plug was taken to be E0.5. Embryos were subsequently harvested on the stipulated day. Germ cells (GFP-positive) and associated somatic cells (GFP-negative) were isolated separately from individual embryos using FACs sorting on the MoFLo XDP or FACS Aria platforms. Live cells, i.e. only those staining negative for propidium iodide, were collected, and typically purity checking on the GFP negative populations was >99%. RNA was isolated from FACs sorted purified cell populations using the Ambion PicoPure RNA isolation kit. Eluted RNA was used to obtain double-stranded-cDNA using the Clontech (SMARTER) Ultralow input RNA-Seq Kit according to the manufacturer’s protocol, or the Smart-Seq2 protocol. cDNA was normalized to 10ng in low-TE buffer and was sheared using Covaris S-series, and was cleaned up with Zymo DNA conc-5 and eluted in 12ul low TE. Libraries of ~300bp were generated 510 using Nugen Ovation® Ultralow DR (part No. 0330) with 15 PCR cycles.

Platform

PlatformILLUMINA
Instrument ModelIllumina HiSeq 2500

Processing

Base Calls
Sequence Space
Base Caller

Spot Information

Number of Reads per Spots0
Spot Length100

Read Spec

Read Index 0
Read Label
Read ClassApplication Read
Read TypeForward
Base Coord1
Read Index 1
Read Label
Read ClassApplication Read
Read TypeReverse
Base Coord51

Navigation

Submission ERA610634 FTP
Study ERP015330
Sample ERS1133990
Run ERR1389167 FASTQ SRA
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