From 3f5399762243c8c18e29729d115b2aff74faa2bc Mon Sep 17 00:00:00 2001 From: Maya Brandi Date: Wed, 26 Nov 2014 07:38:46 +0100 Subject: [PATCH] cleaning --- __init__.py | 72 ----------------------------------------------------- 1 file changed, 72 deletions(-) diff --git a/__init__.py b/__init__.py index 37b0563..e69de29 100644 --- a/__init__.py +++ b/__init__.py @@ -1,72 +0,0 @@ -INITALQCFINISHEDLIB = {'24' : 'Customer Gel QC', - '62' : 'qPCR QC (Library Validation) 4.0', - '64' : 'Quant-iT QC (Library Validation) 4.0', - '67' : 'Qubit QC (Library Validation) 4.0', - '20' : 'CaliperGX QC (DNA)', - '17' : 'Bioanalyzer QC (Library Validation) 4.0'} -INITALQC ={'63' : 'Quant-iT QC (DNA) 4.0', - '65' : 'Quant-iT QC (RNA) 4.0', - '66' : 'Qubit QC (DNA) 4.0', - '68' : 'Qubit QC (RNA) 4.0', - '24' : 'Customer Gel QC', - '20' : 'CaliperGX QC (DNA)', - '16' : 'Bioanalyzer QC (DNA) 4.0', - '18' : 'Bioanalyzer QC (RNA) 4.0', - '116' : 'CaliperGX QC (RNA)', - '504' : 'Volume Measurement QC'} -AGRINITQC = {'7' : 'Aggregate QC (DNA) 4.0', - '9' : 'Aggregate QC (RNA) 4.0'} -PREPREPSTART = {'74': 'Shear DNA (SS XT) 4.0', - '304' : "Ligate 3' adapters (TruSeq small RNA) 1.0"} -POOLING = {'42': "Library Pooling (Illumina SBS) 4.0", - '43': "Library Pooling (MiSeq) 4.0", - '44': "Library Pooling (TruSeq Amplicon) 4.0", - '45': "Library Pooling (TruSeq Exome) 4.0", - '58': "Pooling For Multiplexed Sequencing (SS XT) 4.0", - '255': "Library Pooling (Finished Libraries) 4.0", - '308': "Library Pooling (TruSeq Small RNA) 1.0", - '404': "Pre-Pooling (Illumina SBS) 4.0", - '506': "Pre-Pooling (MiSeq) 4.0", - '508': "Applications Pre-Pooling"} -PREPSTART = {'10' : 'Aliquot Libraries for Hybridization (SS XT)', - '47' : 'mRNA Purification, Fragmentation & cDNA synthesis (TruSeq RNA) 4.0', - '33' : 'Fragment DNA (TruSeq DNA) 4.0', - '407' : 'Fragment DNA (ThruPlex)', - '308': 'Library Pooling (TruSeq Small RNA) 1.0', - '117' : 'Applications Generic Process', - '405' : 'RiboZero depletion'} -PREPEND = {'157': 'Applications Finish Prep', - '109' : 'CA Purification', - '456' : 'Purification (ThruPlex)', - '111' : 'Amplify Captured Libraries to Add Index Tags (SS XT) 4.0', - '406' : 'End repair, size selection, A-tailing and adapter ligation (TruSeq PCR-free DNA) 4.0', - '311': 'Sample Placement (Size Selection)'} -LIBVAL = {'62' : 'qPCR QC (Library Validation) 4.0', - '64' : 'Quant-iT QC (Library Validation) 4.0', - '67' : 'Qubit QC (Library Validation) 4.0', - '20' : 'CaliperGX QC (DNA)', - '17' : 'Bioanalyzer QC (Library Validation) 4.0'} -LIBVALFINISHEDLIB = {'62' : 'qPCR QC (Library Validation) 4.0', - '64' : 'Quant-iT QC (Library Validation) 4.0', - '67' : 'Qubit QC (Library Validation) 4.0', - '20' : 'CaliperGX QC (DNA)', - '17' : 'Bioanalyzer QC (Library Validation) 4.0', - '24' : 'Customer Gel QC'} -AGRLIBVAL = {'8': 'Aggregate QC (Library Validation) 4.0'} -SEQSTART = {'23':'Cluster Generation (Illumina SBS) 4.0', - '26':'Denature, Dilute and Load Sample (MiSeq) 4.0'} - -DILSTART = {'40' : 'Library Normalization (MiSeq) 4.0', - '39' : 'Library Normalization (Illumina SBS) 4.0'} -SEQUENCING = {'38' : 'Illumina Sequencing (Illumina SBS) 4.0', - '46' : 'MiSeq Run (MiSeq) 4.0'} -WORKSET = {'204' : 'Setup Workset/Plate'} -SUMMARY = {'356' : 'Project Summary 1.3'} -DEMULTIPLEX={'13' : 'Bcl Conversion & Demultiplexing (Illumina SBS) 4.0'} - -FINLIB = ['Finished library', 'Amplicon'] -PROJ_UDF_EXCEPTIONS = ['customer_reference','uppnex_id','reference_genome','application'] -SAMP_UDF_EXCEPTIONS = ['customer_name','reads_requested_(millions)','min_reads', - 'm_reads','dup_rm','status_auto','status_manual','average_size_bp','incoming_qc_status'] - -CALIPER={'20' : 'CaliperGX QC (DNA)','116' : 'CaliperGX QC (RNA)'}