THIS IS A NOTICE OF INTENT TO AWARD A SOLE SOURCE CONTRACT AND IS NOT A REQUEST FOR COMPETITIVE QUOTES. Department of Veterans Affairs, Network Contracting Office (NCO) 20, anticipates making a sole source award under statutory authority 41 U.S.C. 253(c) and FAR 13.106-1(b)(1)(i), only one responsible source, with: University of Washington, UW Pathology - Reference Lab, 1959 NE Pacific Street, Seattle, WA 98195. The objective of this sole source award is to procure all the following pathology tests as listed in Tables A-D below. Turnaround time will not exceed 72 hours or 3 working days. The NAICS code for this requirement is 621511. This notice of intent is not a request for competitive quotes; however, interested persons may identify their interest and capability to respond to this requirement. Information received by 11:00 AM Pacific Time on September 16, 2016 may be considered by the Government. Responses shall be submitted to Laura Patterson at [email protected]. The email subject line shall state, "Special Notice Number VA26016Q0964." A determination by the Government not to compete this proposed contract action based upon responses to this notice is solely within the discretion of the Government. Information received will normally be considered solely for the purpose of determining whether to conduct a competitive procurement. NO TELEPHONE REQUESTS WILL BE HONORED. Table A: General Anatomic Pathology Reference Lab Test List CPT Description 84311-TC SPECTROPHOTOMETRY 87491-TC CHLAMYDIA TRACHOMATIS, AMPLIFIED PROBE TECHNIQUE 87591-TC NEISSERIA GONORRHOEAE, AMPLIFIED PROBE TECHNIQUE 87621-TC IADNA PAPLMVIRUS HUMAN AMP PRB 88104-TC CYTP FLU WASHGS/BRUSHINGS XCPT CIV SMRS INTERPJ 88104-26 CYTP FLU WASHGS/BRUSHINGS XCPT CIV SMRS INTERPJ 88108-TC CYTP CONCENTRATION SMRS&INTERPJ 88108-26 CYTP CONCENTRATION SMRS&INTERPJ 88112-TC CYTP SLCTV CELL ENHANCEMENT INTERPJ XCPT CIV 88112-26 CYTP SLCTV CELL ENHANCEMENT INTERPJ XCPT CIV 88120-TC CYTP INSITU HYBRID URINE SPEC 3-5 PROBES EA MNL 88120-26 CYTP INSITU HYBRID URINE SPEC 3-5 PROBES EA MNL 88125-TC FORENSIC CYTOPATHOLOGY 88125-26 FORENSIC CYTOPATHOLOGY 88141-TC CYTOPATH CIV INTERPRET 88142-TC CYTP CIV FLU AUTO THIN MNL PHYS 88143-TC CYTP CIV FLU AUTO THIN MNL SCR&RESCR PHYS 88150-TC CYTOPATH CIV MANUAL 88153-TC CYTOPATH CIV REDO 88160-TC CYTOPATH SMEAR OTHER SOURCE 88160-26 CYTOPATH SMEAR OTHER SOURCE 88162-TC CYTOPATH SMEAR OTHER SOURCE 88162-26 CYTOPATH SMEAR OTHER SOURCE 88164-TC CYTOPATH TBS CIV MANUAL 88165-TC CYTOPATH TBS CIV REDO 88172-TC CYTP FINE NDL ASPIRATE IMMT CYTOHIST STD DX 1ST 88172-26 CYTP FINE NDL ASPIRATE IMMT CYTOHIST STD DX 1ST 88173-TC CYTP FINE NDL ASPIRATE I&R 88173-26 CYTP FINE NDL ASPIRATE I&R 88177-TC CYTP CIV AUTO THIN LYR PREPJ ADEQUACY EA EVAL 88177-26 CYTP CIV AUTO THIN LYR PREPJ ADEQUACY EA EVAL 88182-TC FLO CYTOMETRY CELL CYCLE/DNA ALYS 88182-26 FLO CYTOMETRY CELL CYCLE/DNA ALYS 88184-TC FLO CYTOMETRY CELL SURF MARKER TECHL ONLY 1ST 88185-TC FLOWCYTOMETRY/TC ADD-ON 88230-TC TISS CUL NON-NEO DISORDERS LYMPHOCYTE 88237-TC TISS CUL NEO DISORDERS B1 MARROW BLD CELLS 88239-TC TISS CUL NEO DISORDERS SOLID TUM 88262-TC CHRMSM CNT 15-20 CLL 2KARYOTYP BANDING 88264-TC CHRMSM ANALYZE 20-25 CELLS 88271-TC MOLEC CYTOGENETICS DNA PRB EA 88273-TC MOLEC CYTG CHRMOML ISH 10-30 CLL 88275-TC MOLEC CYTG INTERPHASE ISH ANALYZE 100-300 CLL 88291-26 CHROMOSOME STUDY ADDITIONAL 88302-TC LVL II-SURG PATH GROSS&MCRSCP XM 88302-26 LVL II-SURG PATH GROSS&MCRSCP XM 88304-TC LEVEL III-SURG PATH GROSS&MICROSCOPIC XM 88304-26 LEVEL III-SURG PATH GROSS&MICROSCOPIC XM 88305-TC LVL IV-SURG PATH GROSS&MCRSCP XM 88305-26 LVL IV-SURG PATH GROSS&MCRSCP XM 88307-TC LVL V-SURG PATH GROSS&MCRSCP XM 88307-26 LVL V-SURG PATH GROSS&MCRSCP XM 88309-TC LVL VI-SURG PATH GROSS&MCRSCP XM 88309-26 LVL VI-SURG PATH GROSS&MCRSCP XM 88311-TC DECALCIFICATION PX 88311-26 DECALCIFICATION PX 88312-TC SPECIAL STAINS GROUP 1 MICROORGANISMS I&R EACH 88312-26 SPECIAL STAINS GROUP 1 MICROORGANISMS I&R EACH 88313-TC SPECIAL STAINS GROUP II ALL OTHER I&R EACH 88313-26 SPECIAL STAINS GROUP II ALL OTHER I&R EACH 88314-TC SPECIAL STAINS HISTOCHEMICAL W/FROZEN SECTION 88314-26 SPECIAL STAINS HISTOCHEMICAL W/FROZEN SECTION 88319-TC DETERMINATIVE HCHEM/CCHEM ID NZM EA 88319-26 DETERMINATIVE HCHEM/CCHEM ID NZM EA 88321-26 CONSLTJ&REPRT SLIDES PREPARED ELSEWHERE 88323-TC CONSLTJ&REPRT MATRL REQ PREPJ SLIDES 88323-26 CONSLTJ&REPRT MATRL REQ PREPJ SLIDES 88325-TC COMPREHENSIVE REVIEW OF DATA 88329-TC PATH CONSULT INTROP 88331-TC PATH CONSLTJ SURG 1ST BLK FROZEN SCTJ 1 SPEC 88331-26 PATH CONSLTJ SURG 1ST BLK FROZEN SCTJ 1 SPEC 88332-TC PATH CONSLTJ SURG EA BLK FROZEN SCTJ 88332-26 PATH CONSLTJ SURG EA BLK FROZEN SCTJ 88333-TC PATH CONSLTJ SURG CYTOLOGIC XM 1ST SIT 88333-26 PATH CONSLTJ SURG CYTOLOGIC XM 1ST SIT 88334-TC PATH CONSLTJ SURG CYTOL XM EA ADDL 88334-26 PATH CONSLTJ SURG CYTOL XM EA ADDL 88341-TC IMHISTOCHEM/CYTCHM INIT ANTIBODY STAIN PROCEDURE 88341-26 IMHISTOCHEM/CYTCHM INIT ANTIBODY STAIN PROCEDURE 88342-TC IMCYTCHM TISS IMMUNOPROXIDASE EA ANTB 88342-26 IMCYTCHM TISS IMMUNOPROXIDASE EA ANTB 88346-TC IMFLUOR STD EA ANTB DIR METH 88346-26 IMFLUOR STD EA ANTB DIR METH 88348-TC ELECTRON MIC DX 88348-26 ELECTRON MIC DX 88350-TC IMMUNOFLUORESCENCE PER SPEC ADD SINGL ANTB STAIN 88350-26 IMMUNOFLUORESCENCE PER SPEC ADD SINGL ANTB STAIN 88360-TC TUMOR IMMUNOHISTOCHEM/MANUAL 88360-26 TUMOR IMMUNOHISTOCHEM/MANUAL 88362-TC NRV TEASING PREPJS 88362-26 NRV TEASING PREPJS 88363-TC EXAM & SELECT ARCHIVE TISSUE MOLECULAR ANALYSIS 88365-TC SITU HYBRIDIZATION EA PRB 88365-26 SITU HYBRIDIZATION EA PRB 88368-TC M/PHMTRC ALYS ISH EA PRB MNL 88368-26 M/PHMTRC ALYS ISH EA PRB MNL 88387-TC TISS EXAM MOLECULAR STUDY 88387-26 TISS EXAM MOLECULAR STUDY 88388-TC TISS EX MOLECUL STUDY ADD-ON 88388-26 TISS EX MOLECUL STUDY ADD-ON TC = Technical Component 26 = Professional Component Table B: Northwest Clinical Genomics Lab Test List CPT(s) Test Description 81415 Amyotrophic Lateral Sclerosis (ALS) Exome Panel 81415 Cardiac Arrhythmia Exome Panel 81415 Cardiomyopathy Exome Panel 81415 Comprehensive Cardiac Arrhythmia / Cardiomyopathy Exome Panel 81415 Comprehensive Dementia, Parkinson's, ALS Exome Panel 81415 Dementia Exome Panel 81415 Exome Panel On Demand 81415 Exome Sequence Analysis 81415 Exome Sequence Comparator 81417 Exome Re-evaluation of Previously Obtained Sequence 81415 Genome Sequence Analysis 81426 Genome Sequence Analysis Comparator 81426 Genome Re-evaluation of Previously Obtained Sequence 81415 Parkinson's Disease Exome Panel 81417 REFLEX to Exome Sequencing 81403 or 81479 Testing for Known Pathogenic Variant Table C: Collagen Diagnostic Laboratory Test List Test Name Gene(s) CPT(s) COL1A1 and COL1A2 gDNA Sequencing COL1A1, COL1A2 81408 x 2 Dominant OI Panel COL1A1, COL1A2, IFITM5 81408 x 2, 81479 x 1 Dominant OI Panel plus PLS3 COL1A1, COL1A2, IFITM5, PLS3 81408 x 2, 81479 x 2 Recessive OI Panel plus ALPL CRTAP, FKBP10, LEPRE1, PPIB, PLOD2, SERPINH1, SERPINF1, SP7, SMP1, TMEM38B, WNT1, CREB3L1, ALPL 81479 Autosomal Dominant and Recessive OI Panel COL1A1, COL1A2, IFITM5, PLS3, CRTAP, FKBP10, LEPRE1, PPIB, PLOD2, SERPINH1, SERPINF1, SP7, SMP1, TMEM38B, WNT1, CREB3L1, ALPL 81479 Classical EDS Panel COL5A1, COL5A2 81479 Core EDS Panel COL5A1, COL5A2, COL3A1 81479 Core Familial Aneurysm Panel ACTA2, COL3A1, TGFBR1, TGFBR2, TGFB2, SMAD3, FBN1, MYH11, MYLK, PRKG1, SLC2A10, TGFB3, NOTCH1, SKI, FBN2, FOXE3 81410 Marfan Syndrome and Loeys-Dietz Panel FBN1, TGFBR1, TGFBR2, TGFB2, TGFB3, SMAD3 81479 Extended Marfan-Related Disorders Panel FBN1, TGFBR1, TGFBR2, TGFB2, TGFB3, SMAD3, SKI, FBN2 81479 Alport Panel COL4A3, COL4A4, COL4A5 81408 x 2, 81407 x 1 Hereditary angiopathy/Incracranial hemorrhage COL4A1, COL4A2 81408, 81479 FBN1 genomic sequencing FBN1 81408 COL3A1 genomic sequencing COL3A1 81479 TGFBR1 and TGFBR2 genomic sequencing TGFBR1, TGFBR2 81405 x 2 Bruck Syndrome FKBP10, PLOD2 81479 x 2 Caffey Disease Targeted COL1A1 81403 Hypophosphatasia ALPL 81479 X-Linked Osteoporosis PLS3 81479 EDS type VI Exon 6 COL1A1 and COL1A2 81479 x 2 FKBP14-Related EDS FKBP14 81479 IFITM5 genomic sequencing IFITM5 81479 PLOD1 genomic sequencing PLOD1 81479 ACTA2 genomic sequencing ACTA2 81405 SMAD3 genomic sequencing SMAD3 81479 SLC2A10 genomic sequencing SLC2A10 81479 TGFB2 genomic sequencing TGFB2 81479 TGFB3 genomic sequencing TGFB3 81479 MYH11 genomic sequencing MYH11 81408 MYLK genomic sequencing MYLK 81479 PRKG1 genomic sequencing PRKG1 81479 BMP1 genomic sequencing BMP1 81479 FKBP10 genomic sequencing FKBP10 81479 CREB3L1 genomic sequencing CREB3L1 81479 CRTAP genomic sequencing CRTAP 81479 P3H1 genomic sequencing P3H1 81479 PLOD2 genomic sequencing PLOD2 81479 PPIB genomic sequencing PPIB 81479 SERPINF1 genomic sequencing SERPINF1 81479 SERPINH1 genomic sequencing SERPINH1 81479 SP7/OSX genomic sequencing SP7/OSX 81479 TMEM38B genomic sequencing TMEM38B 81479 WNT1 genomic sequencing WNT1 81479 X-Linked Alport Syndrome COL4A1 81408 Prenatal Testing All genes 81479 Testing for Familial Pathogenic Variant Known Mutation Testing of COL1A1, COL1A2, TGFBR1, TGFBR2, FBN1 and ACTA2 81403 Testing for Familial Pathogenic Variant Known Mutation Testing of all other genes (COL2A1, SMAD3, P3H1, etc.) 81479 Deletion/Duplication Analysis All genes 81228 Deletion/Duplication Analysis (additional gene) G0452 Maternal Cell Contamination Studies 81465 COL1A1 and COL1A2 gDNA Sequencing COL1A1, COL1A2 81408 x 2 Dominant OI Panel COL1A1, COL1A2, IFITM5 81408 x 2, 81479 x 1 Dominant OI Panel plus PLS3 COL1A1, COL1A2, IFITM5, PLS3 81408 x 2, 81479 x 2 Recessive OI Panel plus ALPL CRTAP, FKBP10, LEPRE1, PPIB, PLOD2, SERPINH1, SERPINF1, SP7, SMP1, TMEM38B, WNT1, CREB3L1, ALPL 81479 Classic EDS Panel COL5A1, COL5A2 81479 Alport Panel COL4A3, COL4A4, COL4A5 81408 x 2, 81407 x 1 FBN1 genomic sequencing FBN1 81408 COL3A1 genomic sequencing COL3A1 81479 Table D: Clinical Cytogenomics/Array Lab Test List Test Name Genes CPT(s) Constitutional Cytogenomic Microarray Analysis Whole Genome 81229, G0452 Neoplasia Cytogenomic Microarray Analysis Whole Genome 81229, G0452 Y Chromosome Microdeletion Analysis AMELY, CDY1, DA, DBY, HSFY1, RBMY1, SRY, USP9Y 81403

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