NCRO · Pakistan

One lab, from extraction to interpretation.

NCRO runs molecular diagnostics, PCR, Sanger & NGS sequencing, cell-based bioassays and bioinformatics for research, healthcare, biopharma and agrifood clients — with in-house library prep, PhD-level review, and reports built to be acted on.

100+research & industry groups served
80+assays & sequencing services
4sectors: research, health, biopharma, agrifood
Sample → Report
Sample collectionBlood, tissue, swab, food or environmental sample
Extraction & QCDNA/RNA extraction, Nanodrop, gel electrophoresis
AssayPCR/qPCR, Sanger, NGS library prep, ELISA or bioassay
SequencingIn-house library prep; high-throughput runs outsourced
BioinformaticsVariant calling, annotation, pipeline analysis
ReportPhD-reviewed, clinically or technically annotated

Serving research institutions, hospitals & clinical labs, biopharma/biotech and agrifood industries across Pakistan.

RESEARCH HEALTHCARE BIOPHARMA AGRIFOOD
Who's behind the bench

A team built for the hard cases

Our core team carries a collective 30+ years of experience in biotechnology, NGS and genomics. Eight scientists hold advanced degrees spanning MBBS, PhD, FCPS, DVM and MPhil — clinical, veterinary and research backgrounds working the same bench.

30+ years combined experience in biotechnology, NGS & genomics
8 core scientists on the team
5 degree disciplines: MBBS · PhD · FCPS · DVM · MPhil
What we run

Core laboratory capabilities

Eight service lines under one roof — sample prep through to clinical interpretation.

MBA · MBS

Molecular Diagnostics & PCR

Conventional, multiplex & real-time qPCR, HRM, gene-expression panels and AMR gene panels.

GS

Sanger Sequencing

16S/ITS genotyping and amplicon sequencing with chromatograms, FASTA and BLAST reports.

GS · BDA

NGS & Genomics

In-house library prep for WGS, WES, transcriptomics and metagenomics; high-throughput sequencing outsourced to partner NovaSeq X and DNBSEQ-T7 platforms, analysed in-house.

BDA

Bioinformatics

Variant calling & annotation, phylogenetics, microbiome analysis, protein structure prediction, custom pipelines.

MBS

ELISA & Immunoassays

Quantitative immunoassay development and testing for research and quality-control samples.

PD

Cell-Based Bioassays

Relative potency, neutralization and binding assays for biologics and biosimilars — validated cell-based methods for release and comparability testing.

CG

Clinical Cancer Genomics

Comprehensive genomic profiling, hereditary and tumor-specific panels with ACMG-classified clinical reporting.

WT · CS

Training & Contract Research

Molecular biology and bioinformatics workshops, custom assay development, outsourced R&D.

Clinical Cancer Genomics

Precision oncology, from block to report

Whole exome sequencing analysis services that identify cancer-associated variants, hereditary cancer risk and actionable, precision-oncology findings.

Jump to the gene panel database ↓
Download the Clinical Cancer Genomics brochure (PDF)

Genes covered include

BRCA1 BRCA2 TP53 PALB2 ATM CHEK2 + many more

Deliverables: variant summary, clinical significance, ACMG classification, literature-supported findings, risk assessment and therapeutic implications.

Sample reports

De-identified real case output. Click to preview.

Click a test to see what it covers.

Comprehensive Genomic Profiling (CGP)FFPE / BloodRs. 97,000–115,000

Sequences and analyzes 562 genes associated with solid tumors — SNVs, indels, CNVs, select fusions and genomic signatures, reported against an ACMG-aligned classification framework.

ABL1, ABL2, ACVR1, ACVR2A, AFF3, AKT1, AKT2, AKT3, ALK, ALOX12B, AMER1, ANKRD11, ANKRD26, APC, AR, ARAF, ARID1A, ARID1B, ARID2, ARID5B, ASXL1, ASXL2, ATAD5, ATF1, ATM, ATR, ATRX, AURKA, AURKB, AXIN1, AXIN2, AXL, B2M, BAP1, BARD1, BBC3, BCL10, BCL2, BCL2L1, BCL2L11, BCL6, BCOR, BCORL1, BCR, BIRC3, BLM, BMPR1A, BRAF, BRCA1, BRCA2, BRD3, BRD4, BRIP1, BTG1, BTK, CALR, CAMTA1, CARD11, CASP8, CBFB, CBL, CCND1, CCND2, CCND3, CCNE1, CD274, CD276, CD74, CD79A, CD79B, CDC73, CDH1, CDK12, CDK4, CDK6, CDK8, CDKN1A, CDKN1B, CDKN2A, CDKN2B, CDKN2C, CEBPA, CENPA, CHD2, CHD4, CHEK1, CHEK2, CIC, CNBD1, CNTNAP2, COP1, CREBBP, CRKL, CRLF2, CSF1R, CSF3R, CSMD3, CSNK1A1, CTCF, CTLA4, CTNNA1, CTNNA2, CTNNB1, CTNND2, CUL3, CUX1, CXCR4, CYLD, DAXX, DCC, DDB2, DDR2, DDX41, DICER1, DIS3, DNAJB1, DNMT1, DNMT3A, DNMT3B, DOT1L, DROSHA, E2F3, EED, EGFL7, EGFR, EIF1AX, EIF4A2, EIF4E, ELOC, EML4, EMSY, EP300, EPAS1, EPCAM, EPHA3, EPHA5, EPHA7, EPHB1, ERBB2, ERBB3, ERBB4, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERG, ERRFI1, ESR1, ETV1, ETV4, ETV5, ETV6, EWSR1, EZH2, FAM175A, FAM46C, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FAS, FAT1, FAT3, FBXW7, FGF1, FGF10, FGF12, FGF14, FGF19, FGF2, FGF23, FGF3, FGF4, FGF5, FGF6, FGF7, FGF8, FGF9, FGFR1, FGFR2, FGFR3, FGFR4, FH, FHIT, FIP1L1, FLCN, FLT1, FLT3, FLT4, FOXA1, FOXL2, FOXO1, FOXP1, FRS2, FUBP1, FYN, GABRA6, GATA1, GATA2, GATA3, GATA4, GATA6, GEN1, GID4, GLI1, GNA11, GNA13, GNAQ, GNAS, GPC5, GPR124, GPS2, GREM1, GRIN2A, GRM3, GSK3B, H3F3A, H3F3B, H3F3C, HGF, HIST1H1C, HIST1H2BD, HIST1H3B, HIST1H3C, HIST1H3D, HIST1H3E, HIST1H3F, HIST1H3G, HIST1H3H, HIST1H3I, HIST1H3J, HIST2H3A, HIST2H3D, HIST3H3, HLA-A, HLA-B, HLA-C, HNF1A, HNRNPK, HOXB13, HRAS, HSD3B1, HSP90AA1, ICOSLG, ID3, IDH1, IDH2, IFNGR1, IGF1, IGF1R, IGF2, IKBKE, IKZF1, IL10, IL7R, INHA, INHBA, INPP4A, INPP4B, INSR, IRF2, IRF4, IRS1, IRS2, JAK1, JAK2, JAK3, JUN, KAT6A, KDM5A, KDM5C, KDM6A, KDR, KEAP1, KEL, KIF5B, KIT, KLF4, KLHL6, KMT2B, KMT2C, KMT2D, KRAS, LAMP1, LATS1, LATS2, LMO1, LRP1B, LYN, LZTR1, MAD2L2, MAGI2, MALAT1, MALT1, MAP2K1, MAP2K2, MAP2K4, MAP3K1, MAP3K13, MAP3K14, MAPK1, MAPK3, MAX, MCL1, MDC1, MDM2, MDM4, MED12, MEF2B, MEN1, MET, MGA, MITF, MLH1, MLH3, MLL, MLLT3, MPL, MRE11A, MSH2, MSH3, MSH4, MSH5, MSH6, MST1, MST1R, MTAP, MTOR, MUC16, MUTYH, MYB, MYC, MYCL, MYCN, MYD88, MYOD1, NAB2, NBEA, NBN, NCOA3, NCOR1, NEGR1, NF1, NF2, NFE2L2, NFKBIA, NKX2-1, NKX3-1, NOTCH1, NOTCH2, NOTCH3, NOTCH4, NPM1, NRAS, NRG1, NSD1, NSD2, NSD3, NTRK1, NTRK2, NTRK3, NUP93, NUTM1, PAK1, PAK3, PAK7, PALB2, PARK2, PARP1, PARP2, PARP3, PAX3, PAX5, PAX7, PAX8, PBRM1, PDCD1, PDCD1LG2, PDGFB, PDGFRA, PDGFRB, PDK1, PDPK1, PGR, PHF6, PHOX2B, PIK3C2A, PIK3C2B, PIK3C2G, PIK3C3, PIK3CA, PIK3CB, PIK3CD, PIK3CG, PIK3R1, PIK3R2, PIK3R3, PIM1, PLCG2, PLK2, PMAIP1, PMS1, PMS2, PNRC1, POLD1, POLE, PPARG, PPM1D, PPP2R1A, PPP2R2A, PPP6C, PRDM1, PREX2, PRKAR1A, PRKCI, PRKDC, PRSS8, PSIP1, PTCH1, PTEN, PTPN11, PTPRD, PTPRS, PTPRT, QKI, RAB35, RAC1, RAD21, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RAD52, RAD54L, RAF1, RANBP2, RARA, RASA1, RB1, RBM10, RECQL, RECQL4, REL, RET, RFWD2, RGS7, RHEB, RHOA, RICTOR, RIT1, RNF43, ROBO1, ROBO2, ROS1, RPS6KA4, RPS6KB1, RPS6KB2, RPTOR, RUNX1, RUNX1T1, RYBP, SDHA, SDHAF2, SDHB, SDHC, SDHD, SETBP1, SETD2, SF3B1, SH2B3, SH2D1A, SHQ1, SLIT2, SLX4, SMAD2, SMAD3, SMAD4, SMARCA4, SMARCB1, SMARCD1, SMC1A, SMC3, SMO, SNCAIP, SOCS1, SOX10, SOX17, SOX2, SOX9, SPEN, SPOP, SPTA1, SRC, SRSF2, STAG1, STAG2, STAT3, STAT4, STAT5A, STAT5B, STK11, STK40, SUFU, SUZ12, SYK, TAF1, TBX3, TCEB1, TCF3, TCF7L2, TEK, TERC, TERT, TET1, TET2, TFE3, TFRC, TGFBR1, TGFBR2, TMEM127, TMPRSS2, TNFAIP3, TNFRSF14, TOP1, TOP2A, TP53, TP63, TRAF2, TRAF7, TRRAP, TSC1, TSC2, TSHR, U2AF1, VAV1, VEGFA, VHL, VTCN1, WRN, WT1, XIAP, XPO1, XRCC1, XRCC2, XRCC3, XRCC5, YAP1, YES1, ZBTB2, ZBTB7A, ZFHX3, ZNF217, ZNF703, ZRSR2.
HRD-50 AnalysisFFPE / BloodRs. 100,000–116,000

Not a fixed gene panel — HRD is a genome-wide scarring signature. The Genomic Instability Score (GIS) combines three components measured across the genome:

LOH (loss of heterozygosity) + TAI (telomeric allelic imbalance) + LST (large-scale state transitions). A GIS ≥42 is reported HRD-positive.

Interpreted alongside BRCA1/BRCA2 mutation status to flag PARP-inhibitor and platinum-chemotherapy sensitivity.

BRCA1 & BRCA2 AnalysisFFPE / BloodRs. 98,000–114,000

Genes: BRCA1, BRCA2. Full coding-region and splice-site coverage for germline or somatic pathogenic variants informing hereditary breast/ovarian cancer risk and PARP-inhibitor eligibility.

Microsatellite Instability (MSI)FFPE / BloodRs. 112,000–130,000

Mismatch-repair genes assessed: MLH1, MSH2, MSH6, PMS2 (plus the EPCAM regulatory region). Identifies MSI-High / dMMR tumors eligible for checkpoint-inhibitor immunotherapy.

Tumor Mutational Burden (TMB)FFPE / BloodRs. 117,000–135,000

Computed genome-wide from the sequencing data (mutations per megabase) rather than a fixed gene list — high TMB is an independent biomarker for immune checkpoint inhibitor response.

Germline Hereditary Cancer PanelBloodRs. 120,000

Clinically actionable hereditary cancer genes selected per NCCN hereditary testing criteria, including BRCA1, BRCA2, TP53, PALB2, ATM, CHEK2, MLH1, MSH2, MSH6, PMS2, APC, MUTYH, PTEN, STK11, CDH1 and others.

Precision Oncology Clinical ReportFFPE TissueRs. 147,000

Not a standalone test — a synthesized clinical report integrating CGP, HRD and biomarker findings (MSI, TMB) into a single ACMG-classified, therapy-oriented summary for the treating oncologist.

Tumor-type genomic panels (lung, breast, ovarian, colorectal, pancreatic, prostate, gastric, melanoma) — Rs. 145,000 each, FFPE tissue, 5-week TAT.

Sample reports

Real NCRO case output, de-identified — all patient, physician and institution details removed. Shown to illustrate report depth and format; click a case to expand.

Case A — High-Grade Serous Carcinoma CGP + HRD · FFPE & Blood PIK3CA positive · HRD positive

CGP — FFPE tissue, DNA WES, average coverage 89.03x. Genes tested: BRAF, BRCA1, BRCA2, BRIP1, CHEK1, CHEK2, PALB2, RAD51C, RAD51D, TP53 — all negative.

GeneMutationVAFSignificance
PIK3CAc.G1798A (p.E600K)15.5% (het)Pathogenic

COSMIC ID COSV55891897 — observed in endometrium, cervix and bladder carcinoma samples.

Additional VUS

GeneMutationVAFSignificance
GNASc.G2531A (p.R844H)24.8% (het)Likely Pathogenic

COSMIC ID COSV55670349 — observed in ovarian carcinoma/adenoma/borderline tumors, plus thyroid, soft tissue, small intestine and pituitary cancers.

HRD — Peripheral blood, DNA WES. Status: POSITIVE — GIS 95/100 (threshold ≥42). LOH 41 · TAI 32 · LST 22.

Case B — Peritoneal / Omental Deposit HRD only · Blood (EDTA) HRD positive

HRD — Peripheral blood in EDTA, DNA WES via Agilent SureSelect Human All Exon V6 library prep, sequenced on BGI DNBSEQ; HRD status determined via scarHRD.

Status: POSITIVE — GIS 69/100 (threshold ≥42). LOH 15 · TAI 21 · LST 33.

Case C — Serous Carcinoma CGP + HRD · Blood No pathogenic CGP findings · HRD positive

CGP — Peripheral blood, DNA WES (Agilent SureSelect Human All Exon V6 + BGISEQ), average coverage 130.6x. Genes tested: BRAF, BRCA1, BRCA2, BRIP1, CHEK1, CHEK2, PALB2, RAD51C, RAD51D, PIK3CA, TP53 — all negative.

Variants of uncertain significance

GeneMutationVAFSignificance
BAP1c.1408G>A (p.G470R)42.46% (het)Uncertain significance
FLCNc.1333G>A (p.A445T)47.6% (het)Uncertain significance

BAP1: BAP1 tumor predisposition syndrome (ClinVar 133663 / dbSNP rs576538858). FLCN: Birt-Hogg-Dubé syndrome, colorectal cancer (ClinVar 3370 / dbSNP rs41419545).

HRD — Peripheral blood, DNA WES. Status: POSITIVE — GIS 51/100 (threshold ≥42). LOH 7 · TAI 13 · LST 31.

01

Sample collection

Patient blood or tissue received

02

DNA extraction & QC

High-quality DNA extracted and evaluated

03

Whole exome sequencing

All protein-coding regions sequenced

04

Bioinformatics analysis

Computational variant identification

05

Clinical interpretation

Variant annotation, significance assessment

06

Comprehensive reporting

Customized report per client requirements

Whole blood (germline)

  • 3–5 mL peripheral blood
  • EDTA (purple-top) tube
  • Store at 2–8°C
  • Ship within 48 hours

FFPE tissue (block)

  • Submit clearly labeled block
  • Include pathology report if available
  • Somatic variant / solid tumor profiling

Fresh tissue

  • Sterile container
  • Keep chilled, 2–8°C
  • Ship immediately
  • Avoid freeze-thaw cycles

Purified DNA

  • ≥500 ng high-quality genomic DNA
  • A260/A280 ratio 1.8–2.0
  • Concentration ≥20 ng/µL

Search the gene panel database

4,953 unique genes across NCRO's nine curated panels — PanCancer Pro, Hemato Pro, Neoscreen Pro, Cardio Pro, ClinEX Pro, Fusion Pro, Heva Pro, HRD Pro and IVF Pro — each with its clinical or research significance and, where one exists, the FDA-approved drug or NCCN-aligned clinical management implication. A gene relevant to more than one panel is listed once, with the panel-specific significance merged in. Want to build a custom Sanger, PCR or NGS order around specific genes or exons, or get an instant priced quote? Visit NCRO Biotools (login required).

Gene
Panel
Clinical / research significance
Therapeutic / clinical note
No genes match that search.

Drug and clinical-management information reflects FDA approvals and NCCN-aligned practice at the time of writing and is for reference only — always confirm current guidance and eligibility with the treating oncologist.

Diagnostics Panel

AMR Gene Panel

Detect today. Treat right. Protect tomorrow. A conventional PCR-based panel detecting a wide range of antimicrobial resistance genes across major bacterial pathogens — covering beta-lactams, carbapenems, aminoglycosides, fluoroquinolones, macrolides, tetracyclines and sulfonamides, including ESBL, AmpC, carbapenemase and MBL resistance genes.

ESBLAmpCCarbapenemasesMBL
Food testingProduct safety & recall risk
Microbiology labsIsolate surveillance
EnvironmentalWater, soil & waste monitoring

NCRO-MBA-AMR12 · 12-gene PCR assay · Rs. 26,000

Download the AMR Gene Panel brochure (PDF)
Better data.
Better decisions.
Better outcomes.
CONVENTIONAL PCR · VALIDATED PRIMERS
Resistance Gene Reference

AMR gene & species database

43 antimicrobial resistance genes spanning ESBL, AmpC, carbapenemase/MBL, aminoglycoside, fluoroquinolone, macrolide, tetracycline, sulfonamide, glycopeptide/MRSA and colistin resistance mechanisms, mapped to the organisms they're most commonly found in.

Gene
Resistance class
Mechanism
Associated species
No genes match that search.

Species listed reflect the organisms this gene is most commonly detected in — not an exhaustive host range. Panel composition can be tailored per client (clinical, food safety or environmental surveillance use case).

Protein & Cell Biology

Cell-based potency & bioassay services

Relative potency testing for biologics and biosimilars, run as validated cell-based assays with tiered sample packages. Custom assay development available for other molecules.

Jump to the biologics database ↓

Adalimumab

TNF-α neutralization assay
Package 1 · 1 sampleRs. 810,000
Package 2 · 2 samplesRs. 815,000
Package 3 · 3 samplesRs. 1,100,000

Trastuzumab

BT-474 anti-proliferation assay
Package 1 · 1 sampleRs. 805,000
Package 2 · 2 samplesRs. 810,000
Package 3 · 3 samplesRs. 1,090,000

Rituximab

Complement dependent cytotoxicity (CDC)
Package 1 · 1 sampleRs. 1,575,000
Package 2 · 2 samplesRs. 1,600,000
Package 3 · 3 samplesRs. 2,135,000

Bevacizumab

VEGF neutralization assay
Package 1 · 1 sampleRs. 825,000
Package 2 · 2 samplesRs. 830,000
Package 3 · 3 samplesRs. 1,111,000

Packages are priced per sample set (samples + reference standard, run in triplicate). Turnaround and payment terms confirmed at quotation stage.

Assay Reference Database

Biologics potency assay database

60 innovator biologics and their approved biosimilars, organized by drug class, with the test method and generic reference cell line for each — brand-agnostic, so it reflects what's biologically being tested rather than a specific reagent vendor. Search or filter by class to check what we can run.

Drug class
Innovator (reference product)
Approved biosimilars
Test method & generic cell line
No biologics match that search.

Reference cell lines are generic/brand-agnostic (e.g. GenScript catalog IDs), listed only where a validated line is available; most classes are run as custom cell-based potency assays. Not all molecules are stock-held — confirm availability when requesting a quote.

The Ledger

Search the service catalogue

Every listed service carries its own catalogue number, unit and indicative price — search or filter by category to find what you need.

Catalogue No.
Service
Unit
Price
No services match that search.

Prices in PKR, exclusive of applicable sales tax. Volume, panel and multi-sample pricing available on request — request a formal quotation.

Downloads

Resource library

Brochures and de-identified sample reports — browse or download directly. Search to filter by name or category.

No resources match that search.

Need something that isn't listed — a proposal, an SLA, a custom panel spec? Request it here and we'll send it over.

Who we work with

Built for four industries

01

Research & academia

Universities and institutes running genomics, molecular biology and bioinformatics projects.

02

Healthcare

Hospitals and clinics referring hereditary, infectious disease and oncology molecular testing.

03

Biopharma & biotech

Potency, comparability and characterization testing for biologics and biosimilars.

04

Agrifood & environment

Pathogen panels, GMO detection, food safety and environmental molecular testing.

How we work

From email to report

01

Send your brief

Email us a short overview of the project or sample you need tested.

02

Scientific assessment

Our PhD-level team reviews it and prepares a proposal.

03

Consultation

We meet to discuss the proposal and finalize scope.

04

Sample submission

Samples are shipped or collected per our logistics guidance.

05

Testing & analysis

Assay, sequencing and bioinformatics work is carried out.

06

Report delivered

A reviewed, actionable report is sent to your team.

Benefited by many

Used by more than 100 groups

"We have utilized this group's services and have always felt satisfied with the results."

Prof. Dr. Khan

"Wonderful service — on time and on budget. We recommend this service to anyone interested in serious and quality research."

Prof. Niazi
Get in touch

Book a free consultation

Send us a brief overview of your project — our scientific team will review it and get back with a proposal.