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CHPC awards allocations on the general resources of the kingspeak and ember clusters based on proposals submitted to a review committee. The allocation is awarded to the CHPC PI, and access to the allocation is made available to all members of the group. Jobs from groups with allocation run at a higher priority and can preempt jobs running without allocation. Note that lonepeak general nodes are run in an unallocated manner.

Other resources on the clusters are "owned" by other PIs and your jobs will not be able to run on those nodes at priority unless you are a member of that group. You may run on the "owner nodes" by changing the SBATCH directives for the account and partition as desciribed on the leather biker jacket mens hm denim jacket with fur
. Your job can thus be run on any idle owner nodes, at low priority, but your job can be pre-empted (killed) if a member of the owner's group submits a job.

at priority

Allocations are measured in wallclockcore hour which are 1 hour of wallclock time for each core on a node. For more details see our HPC Allocation Policy . Allocations are managed on a calendar quarter.

wallclockcore hour for each core

There are two kinds of allocation:

Quick allocations are for PIs who are new to having a CHPC allocation. PIs may submit a quick allocationrequest which is for 20,000 wallclock core hours for the current calendar quarter at any time during the quarter. It is expected that after gaining experience using our systems with the quick allocation, the allocation process (below) should be followed. Quick allocations are reviewed by senior CHPC staff and awarded at CHPC's discretion.

Requests for allocations are accepted 4 times per year. The due dates for the four opportunities are set each quarter:

The exact dates are set each quarter and announced through the chpc-hpc-users mailing list. The maximum award amount is 200,000.

PIs are asked to submit a request for the four upcoming calendar quarters. Your allocation request will then need to be renewed the following year by submitting another request. You may ask for fewer quarters, but if you expect to be using our systems long term we request that you submit a full year request. If you find your allocation amount needs to be adjusted, you can submit a new request to replace your existing request at any allocation cycle during the year.

Contact CGI: Contact Us | Email


Mature B-cell neoplasms arise in B-cells that have entered germinal centers within lymph nodes as part of the immune response. They display great heterogeneity at the clinical, pathologic, and genetic levels and represent 6-7% and 5-6% of all new estimated cancer cases and deaths respectively in the US in 2009. They are the fifth most common neoplasm in both males and females, and of the 103,960 estimated new cases in 2009, 20,860 comprise diffuse large B-cell lymphoma (DLBCL), 20,580 multiple myeloma (MM), 15,490 chronic lymphocytic leukemia /small lymphocytic lymphoma (CLL/SLL), 14,900 follicular lymphoma (FL), 8,510 Hodgkin’s lymphoma (HL), 6,000 marginal zone lymphomas (MZL) (including the three subtypes: extranodal marginal zone of mucosa-associated lymphoid tissue [MALT], nodal marginal zone, and splenic marginal zone), and 3,730 mantle cell lymphomas (MCL), as the major subtypes. With the exclusion of HL, 32,520 deaths are expected in 2009 in the US as a result of these neoplasms.

Diagnosis of these neoplasms relies mostly on the pathologic examination of biopsy material, be it either of an incisional or excisional biopsy of a suspect lymph node, a fine needle aspirate of a suspect lymph node (as yet to be considered adequate for initial diagnosis, unless it is the only safe option), or a bone marrow aspirate. Unlike other cancers, rarely are other biopsy/surgical procedures performed prior to the initiation of treatment, thus limiting the amount of tissue available for diagnostic and prognostic purposes. CGI has optimized the utility of array-CGH so that it can be routinely applied to the study of a range of specimen types including formalin-fixed paraffin-embedded (FFPE) specimens, often the only specimen available for analysis.

CGI has designed an oligonucleotide-based array (MatBA®) for the detection of gains and losses in mature B-cell neoplasms for utilization within a clinical laboratory.

For CLL/SLL, it’s primary value is in routine prognostication, and as an assay, has been approved in the CGI Diagnostic Laboratory by both CLIA and New York State. In this disease where approximately 50% patients have an aggressive course and 50% can live for many years without requiring treatment, robust prognostication is highly desirable. Together with IGHV mutation status, theMatBA®-CLL Array-CGH test provides important genetic-based information to guide clinical management of this disease.

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Press Release
April 7, 2018

April 3, 2018 ስለ ዶክተር ዓብይ አህመድ የኢትዮጵያ ጠቅላይ ሚኒትር ሆኖ በመመረጡ ከአፋር ነፃ አውጪ ግንባር ፓርቲየወጣ መግልጫ። የኢትዮጵያ ሕዝብ ፍትህና እኩልነት የናፈቀው በመሆኑ በኣዲሱ ጠቅላይ ሚኒስትር መመረጥ ደስታውን እየገልጸ ይገኛል። የኣፋር ነጻ አውጭ ግንባር [Read More]

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OLF’s Position on the Solution

April 5, 2018

OLF’s Position on the Solution to the current Political Crisis in Ethiopia Press release (Oromo Liberation Front) To end the current political crises peacefully, OLF once again would like to show its readiness for negotiation. [Read More]

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OLF ALFP Joint Statement

March 29, 2018

Instigating an ethnic conflict is an act of State Terrorism in Ethiopia Joint Statement of Afar Liberation Front Party (ALFP) and Oromo Liberation Front (OLF) on current Political Situation of [Read More]

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