GC3F-TS-1242 - GyLib1 - ddRAD

Run Info

Start / End: -

Submitter Info

Lab: Chiba, Satoshi (Tohoku) Lab

Service

Service Requested
HiSeq 4000
Read Type
Single
Length Allowed
100
Length Preferred
100

Details

Fragment Size From
300
Fragment Size To
500
Volume Submitted (µL)
25
Measured Concentration
3.01
Method for Measuring Concentration
Fluorometer
Primer Kit
Illumina TruSeq kit for DNA (24 indices)
Concentration units
ng/µL
Multiplexed?
YES: Contains inline barcodes with NO index reads required
Custom primers requested?
No

Sample

Expected Date Sample will be Submitted

Payment

Comments
I constructed the ddRAD library based on the protocol described in Peterson et al. (2012: Plos One). No modifications to standard sequencing protocols are necessary. All sequencing primers and flowcell annealing sequences are identical to those in standard Illumina multiplexing libraries.

iLab

iLab State
completed
Lab
Chiba, Satoshi (Tohoku) Lab