Current Queue

The Illumina HiSeq 2500 Sequencer has two run modes: the High Output (HO) mode and the Rapid Run (RR) mode. The HO Mode is more cost-effective, yet it takes longer to run and our users need to wait until all 8 lanes of a HO flow cell are filled up. To help our users plan their runs, we provide the following track form for lane use.

Filled lanes represent completed libraries that are ready for sequencing and tentative lanes represent samples currently in preparation. The client's corresponding quote number is also included in the queue. 

If you need faster service, please contact us for a Rapid Run or a MiSeq run. An RR flow cell has only two lanes to fill and can sequence up to 250 nucleotides (instead of 100 nucleotides of a HO run).

     SR50: Single Read 50 bp      SR100: Single Read 100 bp      PE50: Paired End 50 bp      PE100: Paired End 100 bp

 

Sequencing Queue for HiSeq 2500 High Output/Rapid Run Modes and MiSeq

(Updated on 04/25/2017)​​

 


 

Currently Running on HiSeq: 

Next in Queue for HiSeq HO/RR Mode: 

Queue for HiSeq HO/RR Mode: 

 


 

Currently Running on MiSeq: 

Next in Queue for MiSeq: 

Queue for MiSeq: MSv2-PE150 (LZ)

 


 

Lanes on Next HiSeq 2500 HO Flow Cells 

Run Format 1 2 3 4 5 6 7 8

HO SR-50

Filled (Q#-JB) Filled (Q#-JB) Filled (Q#-JB) Filled (Q#-JB) Filled (Q#-JB) Filled (Q#-JB) Empty​ Empty​
HO SR-100

Filled (Q#280-JM)

Filled (Q#280-JM)

Filled (Q#278-MU)

Empty

Empty

Empty

Empty

Empty

HO PE-50

Empty Empty Empty Empty Empty Empty Empty Empty
HO PE-100

Filled (Q#-KC)

Empty

Empty

Empty

Empty

Empty

Empty

Empty

  

Lanes on Next HiSeq 2500 RR Flow Cells 

if both lanes are not purchased, a cBot clustering fee will be added to the lane cost, see services pricing list

Run Format 1 2
RR SR-50 Empty Empty
RR SR-100 Empty Empty
RR SR-150 Empty Empty
RR SR-200 Empty Empty
RR SR-250 Empty Empty
RR PE-50 Empty Empty
RR PE-100 Filled (Q#-KC) Empty
RR PE-150 Empty Empty
RR PE-200 Empty Empty
RR PE-250 Empty Empty

 


CMADP Events

Special seminar by Dr. Kevin W. Plaxco
Professor of Chemistry & Biochemistry
UC Santa Barbara

Wednesday, April 19, 2017 at 4:00pm
School of Pharmacy, Room 3020

"Counting molecules, dodging blood cells: real-time molecular measurements directly in the living body"
The development of technology capable of continuously tracking the levels of drugs, metabolites, and biomarkers in situ in the body would revolutionize our understanding of health and our ability to detect and treat disease. It would, for example, provide clinicians with a real-time window into organ function and would enable therapies guided by patient-specific, real-time pharmacokinetics, opening a new dimension in personalized medicine. In response my group has pioneered the development of a “biology-inspired” electrochemical approach to monitoring specific molecules that supports real-time measurements of arbitrary molecular targets (irrespective of their chemical reactivity) directly in awake, fully ambulatory subjects.
KU Today