| Run | Spots | Bases | Size | GC content | Published | Access Type |
|---|---|---|---|---|---|---|
SRR6780151 |
43.0M | 8.7Gbp | 6.3G | 45.4% | 2019-03-01 | public |
This run has 2 reads per spot:
| L=101, 100% | L=101, 100% |
- Legend
Technical read Application Read L=4, 100% Length is 4, 100% spots contain this read ̅L=165, σ=92.8, 66% Average length is 165, standard deviation is 92.8, 66% spots contain this read
| Experiment | Library Name | Platform | Strategy | Source | Selection | Layout | Action |
|---|---|---|---|---|---|---|---|
| SRX3740153 | R303_rep2 | Illumina | RNA-Seq | TRANSCRIPTOMIC | PCR | PAIRED |
| Biosample | Sample Description | Organism |
|---|---|---|
| SAMN08580358 (SRS2996861) | Total RNA libraries were prepared using isolated total RNA according to the protocol of Illumina TrueSeq RNA Library Preparation Kit (https://support.illumina.com/). The protocol includes purification and fragmentation of mRNA, first stand cDNA synthesis followed by second stand cDNA synthesis, end-repairing of the cDNA, 3 end adenylation, followed by adapter ligation and PCR amplification. The libraries were checked for the average mean size (260 bp) on Agilent DNA 1000 chip using Agilent 2100 Bioanalyzer. The library concentration was checked using Qubit Fluorometer. After obtaining the Qubit concentration for each of the respective libraries, cluster generation was performed using Illumina CBot instrument and finally loaded onto Illumina HiSeq 1000 platform for paired-end sequencing. | Cajanus cajan |
| Bioproject | SRA Study | Title |
|---|---|---|
| PRJNA435480 | SRP133410 | Cajanus cajan isolate:11A_rep1 | cultivar:AKCM11 Raw sequence reads |
Total RNA libraries were prepared using isolated total RNA according to the protocol ofIllumina TrueSeq RNA Library Preparation Kit (https://support.illumina.com/). The protocolincludes purification and fragmentation of mRNA, first stand cDNA synthesis followed bysecond stand cDNA synthesis, end-repairing of the cDNA, 3 end adenylation, followed byadapter ligation and PCR amplification. The libraries were checked for the average mean size(260 bp) on Agilent DNA 1000 chip using Agilent 2100 Bioanalyzer. The libraryconcentration was checked using Qubit Fluorometer. After obtaining the Qubit concentrationfor each of the respective libraries, cluster generation was performed using Illumina CBotinstrument and finally loaded onto Illumina HiSeq 1000 platform for paired-end sequencing.
SRA archive data
SRA archive data is normalized by the SRA load process and used by the SRA Toolkit to read and produce formats like FASTQ, SAM, etc. The default toolkit configuration enables it to find and retrieve SRA runs by accession.
Public SRA files are now available from GCP and AWS cloud platforms as well as from NCBI. Access to most data in the cloud requires a user account with the cloud service provider. The user’s account will incur costs for cloud compute or to copy data outside of the specified cloud service region.
| Type | Size | Location | Name | Free Egress | Access Type |
|---|---|---|---|---|---|
| SRA Lite | 2,206,230 Kb | NCBI | https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-14/SRR006/780/SRR6780151.sralite.1 | worldwide | anonymous |
| AWS | s3://sra-pub-zq-1/SRR6780151/SRR6780151.sralite.1 | s3.us-east-1 | aws identity | ||
| GCP | gs://sra-pub-zq-104/SRR6780151/SRR6780151.zq.1 | gs.us-east1 | gcp identity | ||
| SRA Normalized | 6,177,971 Kb | AWS | https://sra-pub-run-odp.s3.amazonaws.com/sra/SRR6780151/SRR6780151 | worldwide | anonymous |
Original format
The original files submitted to SRA. These files may require specific software to open, read and interpret data.
| Type | Size | Location | Name | Free Egress | Access Type |
|---|---|---|---|---|---|
| fastq | 4,434,857 Kb | AWS | s3://sra-pub-src-6/SRR6780151/R303_rep2_R2.fastq.gz | - | Use Cloud Data Delivery |
| fastq | 4,378,688 Kb | AWS | s3://sra-pub-src-6/SRR6780151/R303_rep2_R1.fastq.gz | - | Use Cloud Data Delivery |
- Egress and Access: what does it mean?
-
Egress
term used by cloud providers to describe cost (charged to the user) of moving data outside of the storage region Free Egresscolumn indicates where the data can be accessed without an egress charge: - worldwide can be downloaded from anywhere for free
- s3.us-east-1 is free to access from machines running in Amazon's us-east-1 region, access from other regions or transport outside of AWS will require paying egress charges
- gs.US is free to access from machines running in Google’s gs.US region, access from other regions or transport outside of GCP will require paying egress charges
Access Typedescribes whether a cloud service user account is necessary for data access. "anonymous" access means general public access Namecolumn provides either a link to free download location at NCBI or a URL for the cloud provider storage location. Either s3:// for Amazon or gs:// for Google storage
- Why is SRA data in the cloud?
-
In order to support large scale (hyper parallel) data analyses SRA data is now available at GCP and AWS with few caveats:
- SRA data is copied to the cloud from NCBI. There may be a lag between availability from NCBI and from CSP (cloud service providers)
- To access public data user account with the cloud service provider is required. Your account will incur costs for cloud compute and/or to copy data (either archival or results of your comute) outside of the specified cloud service region
- Distribution of protected data is signed by NIH account and requires user to operate in the same region as the data
SRA has also begun to provide access to originally submitted source files:
- not all files have been validated by SRA
- not all files have been copied to cloud locations (recovering it from NCBI tape system takes time ).
- the volume of this type of data a much larger and it is not used as often so we will keep most of it on tape or "cold" storage in cloud. As a result the data may not be available instantly and restore requests will be served on first-come first-served basis and cost of resore may be charged to your user account.
- What is "Cloud Data Delivery"?
-
Please visit SRA Data Delivery service to request Sequence Read Archive (SRA) data to be delivered to an Amazon Web Services (AWS) or Google Cloud Platform (GCP) bucket of your choice.
Taxonomy Analysis
- Unidentified reads: 13.34%
- Identified reads: 86.66%
Strong signals
| SuperKingdom | Organism | Rank | %% | Kbp | Coverage |
|---|---|---|---|---|---|
| Eukaryota | Cajanus cajan | species | 86.1 | 7,467,213 | |
| Bacteria | Acinetobacter indicus | species | 0.1 | 8,907 | 2.8 |
| Eukaryota | Glycine max | species | 0.1 | 8,832 | |
| Bacteria | Acinetobacter schindleri | species | 0.0 | 3,434 | 1.1 |
| Bacteria | Acinetobacter lwoffii | species | 0.0 | 2,891 | 0.9 |
| Bacteria | Acinetobacter sp. VT 511 | species | 0.0 | 2,414 | |
| Bacteria | Acinetobacter calcoaceticus/baumannii complex | species group | 0.0 | 1,818 | |
| Bacteria | Acinetobacter idrijaensis | species | 0.0 | 1,607 | |
| Bacteria | Brevundimonas | genus | 0.0 | 1,523 |
- How to read results?
Results show distribution of reads mapping to specific taxonomy nodes as a percentage of total reads within the analyzed run. In cases where a read maps to more than one related taxonomy node, the read is reported as originating from the lowest shared taxonomic node. So when a read maps to two species belonging to the same genus, it is assigned at the genus level. Sequence reads from a single organism will map to several taxonomy nodes spanning the organism’s lineage. The number of reads mapping to higher level nodes will typically be greater than those that map to terminal nodes.
STAT results are proportional to the size of sequenced genomes. Given a mixed sample containing several organisms at equal copy number, proportionally more reads originate from the larger genomes. This means that the percentages reported by STAT will reflect genome size and must be considered against the genomic complexity of the sequenced sample.
- How can I query this analysis data?
Please take a look at NCBI SRA Cloud-based Taxonomy Analysis Table