NgsAdvisory
01Physician-led clinical intelligence

Your NGS report decoded.
Your treatment strategy refined.

A molecular second opinion in oncology. We transform complex genomic sequencing data into clear, actionable clinical recommendations—bridging the gap between laboratory findings and treatment decisions.

130+
Peer-reviewed publications
Prof. İbrahim Yıldız, MD
Phase 3
Principal Investigator
international trials
3 days
Median delivery
48–72 h with priority
ASCO · ESMO
Active membership
current guideline literacy
02The translation

Raw genomic data is noise.
Our job is to make it signal.

5 STAGES · SCROLL TO ADVANCE
What happens here

Raw NGS Output

Hundreds of variants across DNA, RNA, protein. Annotation thin or absent. Clinical relevance unsorted.

chr7:55249071 EGFR L858R AF=0.42 DP=820
chr12:25398284 KRAS G12C AF=0.31 DP=1024
chr17:7577538 TP53 R248Q AF=0.55 DP=910
chr3:178936091 PIK3CA E545K AF=0.18 DP=702
chr2:209113112 IDH1 R132H AF=0.04 DP=68 *low
chr1:115256530 NRAS Q61K AF=0.02 DP=45 *low
chrX:48649700 GATA1 P153L AF=0.49 DP=812 *germ
chr5:112175770 APC I1307K AF=0.51 DP=801 *germ
chr11:534242 HRAS G13R AF=0.03 DP=55 *low
chr10:89717672 PTEN R130G AF=0.21 DP=410
What happens here

Filter

Strip artifacts, germline noise, low-coverage calls. Retain candidates with somatic confidence.

Input · 184 variants
Output · 22 candidates
What happens here

Prioritize

Rank by oncogenic role, allele frequency, pathway position, and clinical actionability score.

EGFR L858R
96
Driver
KRAS G12C
91
Driver
TP53 R248Q
64
Co-occurring
PIK3CA E545K
52
Modifier
PTEN R130G
38
Passenger
What happens here

Interpret

Match each driver to FDA labels, guideline rec's, trials, and emerging literature. Tier 1 / 2 / 3.

FGFR2-VCL fusion
Tier 1
Futibatinib · pemigatinib (FDA-approved)
NCCN · ESMO · MOUNTAINEER
EGFR L858R
Tier 2
Osimertinib (1L NSCLC) — FLAURA evidence
FDA · NCCN Cat 1
PIK3CA E545K
Tier 3
Emerging — alpelisib + endocrine combo
Off-label
What happens here

Decide

Physician-reviewed roadmap: 1L → 2L → 3L+ with anticipated resistance and trial alternatives.

1L
Osimertinib
EGFR L858R · FDA · 12–18 mo
2L
Amivantamab + chemo
If T790M+ resistance · 6–9 mo
3L+
Trial enrollment
HLA-A*02:01 · NCT0XXXX ·
Physician-reviewed
Every roadmap signed off by a board-certified oncologist.
Multi-modal
DNA · RNA · protein-level findings unified into one view.
Trial-aware
Molecular + HLA matching to active enrollment.
03Multi-platform reality

DNA alone misses what changes lives.

Many oncologists order only a DNA-based NGS panel. We integrate DNA · RNA · protein (IHC) · germline — because a single missing layer can hide a Tier IA finding.

Real case · anonymized

Cholangiocarcinoma · 40 yo

A 648-gene DNA panel returned zero actionable variants. On paper, the tumor had no therapeutic targets.

RNA fusion analysis detected an FGFR2-VCL fusion—a Tier IA finding with two FDA-approved therapies (futibatinib, pemigatinib).

DNA panels miss intronic-breakpoint fusions outside probe coverage.
RNA detects the transcript regardless of breakpoint location.

DNA panel · 648 genes
Standard tumor profiling — fusion missed
Zero actionable
RNA fusion panel
Tier IA · futibatinib · pemigatinib
FGFR2-VCL detected
Protein / IHC
Phenotypic corroboration
FGFR2 overexpression confirmed
Germline
Sporadic · no familial workup needed
No pathogenic variant
Without RNA testing, this patient's only treatment option would have been missed entirely.
04The translation, side by side

The report you receive today.
The roadmap we deliver instead.

What you get from the lab
BEFORE
Raw variant report
LAB REPORT — variant table screenshot
  • Long variant tables — driver and passenger undifferentiated
  • Annotation thin · clinical relevance unscored
  • No therapy sequencing · no resistance plan
  • Trial mentions generic, not HLA-matched
What NGS Advisory delivers
AFTER
Treatment roadmap
NGS ADVISORY ROADMAP — physician-reviewed strategy
  • Prioritized drivers — actionability scored 0–100
  • Tier 1/2/3 evidence framework on every recommendation
  • Sequenced 1L → 2L → 3L+ with anticipated resistance
  • HLA + molecular trial matching · physician-signed
05Signature system · 01

Precision Targeting.
Drivers at the center. Context in the periphery.

HOVER ANY MUTATION
CASE NSCLC · 04
Selected · driver
SCORE 96
EGFR
L858R
Oncogenic driver. High allele frequency, established pathway. Direct treatment implication.
Allele Freq · 0.42 Coverage · 820× Tier 1
Driver
Co-occurring
Modifier
Passenger
06Signature system · 02

Treatment as a journey
not a list of drugs.

CASE 04 · NSCLC · ANONYMIZED
Time axis
Diagnosis
Month 6
Month 18
Month 24
On-trial
1L
Anticipated resistance
T790M emergence · MET amplification · histologic transformation
2L
Anticipated resistance
C797S · MET-independent escape
Alt branch · if T790M+ only
Repeat osimertinib + chemo
FLAURA-2 evidence
Evidence basis
3L+
Anticipated resistance
Monitor ctDNA every 8 wks
→ Click any line of therapy to expand evidence + resistance plan.
07Signature system · 03

Evidence in strata.
So physicians always know how strong the ground is.

3 TIERS · CLICK TO PEEL BACK
EGFR L858R
Osimertinib (1L NSCLC)
FDA · NCCN Cat 1 · ESMO IA
BRAF V600E
Dabrafenib + Trametinib
FDA · NCCN Cat 1
KRAS G12C
Sotorasib · matched NCT0XXXXXX
Phase II · NEJM
MET amp
Capmatinib (acquired resistance)
GEOMETRY · Phase II
PIK3CA E545K
Alpelisib + endocrine combo
Off-label · case series
PTEN R130G
PI3K-axis modulation under study
Preclinical
08Our expertise

Six steps beyond the standard report.

Standard NGS reports list mutations and mention drug matches. We add six layers your treating oncologist can act on immediately.

01

Variant Tier Classification

Every variant graded Tier IA → IV per current NCCN, MSK OncoKB, and FDA — and re-graded against your tumor type. A mutation that is Tier IA in lung may be Tier II elsewhere. We make that distinction explicit.

02

Immunotherapy Suitability Score

A quantitative IO score from five parameters: TMB · MSI · PD-L1 · active driver penalty · ultra-low TMB penalty. Positive = IO candidate. Zero or negative = IO not recommended as monotherapy.

03

Treatment Sequencing 1L → 2L → 3L+

Cancer treatment is a sequence, not a decision. Preferred 1L with alternatives, 2L matched to expected resistance, 3L+ with experimental and trial options — each annotated with ORR, PFS, OS evidence.

04

Anticipatory Resistance Strategy

A 4-step plan: (1) what to test at progression, (2) which resistance mutations to expect, (3) which next-gen agents address each, (4) which trials to reserve. For FGFR2 — V564F, N549K · tinengotinib · lirafugratinib.

05

Clinical Trial Matching

Independent, real-time matching against ClinicalTrials.gov and institutional databases. Molecular + HLA + geography (Türkiye, Balkans, EU prioritized). NCT, phase, city, and exact eligibility per match.

06

First-Person Physician Commentary

Every report includes a dedicated commentary written in the first person by Prof. İbrahim Yıldız — a clinical letter your treating oncologist can act on directly, in plain language.

09How it works

From NGS upload to clinical advisory.

A streamlined, secure process for both referring oncologists and patients seeking molecular second opinions.

1
Step 01

Upload your NGS

Send your NGS report (Tempus, FoundationOne, Guardant, Caris, or any panel) via our secure portal with basic clinical context.

2
Step 02

Multi-platform analysis

DNA · RNA · protein · IHC integrated. Cross-referenced with current NCCN guidelines, FDA approvals, and active clinical trials.

3
Step 03

Expert review

Prof. İbrahim Yıldız personally reviews every case — validating tier classifications, treatment recommendations, and trial matches.

4
Step 04

Report delivery

Two documents within 48–72 h: the structured IYGAS™ advisory and the physician commentary. Optional video consultation.

10Deliverables

Two documents.
One complete picture.

Every consultation produces two complementary reports — a structured English-language molecular advisory and a physician commentary in your preferred language.

IYGAS™ Molecular Advisory

14 SECTIONS
  • 01 Patient demographics & specimen context
  • 02 Executive clinical summary · critical findings
  • 03 Genomic & biomarker profile (all platforms)
  • 04 VAF & clonality interpretation model
  • 05 Auto-tier classification (IA → IV)
  • 06 Treatment decision matrix (1L / 2L / 3L+)
  • 07 Immunotherapy suitability score
  • 08 4-step resistance management strategy
  • 09 Pharmacogenomics · dose & toxicity
  • 10 Drug interactions vs. planned therapy
  • 11 Clinical trial matching framework
  • 12 VUS registry with biological context
  • 13 Evidence library & literature support
  • 14 Physician advisory conclusion + signature

Physician Commentary

MULTILINGUAL
  • First-person clinical narrative by Prof. Yıldız
  • "Why this finding matters" — explained, not just listed
  • "Why I recommend this treatment" — with evidence rationale
  • "Why immunotherapy is/isn't appropriate" — IO score explained
  • VUS interpretation with biological mechanism
  • Clinical trial recommendations with eligibility context
  • Age/gender-specific considerations (fertility, germline)
  • Available in TR · EN · BG · RO · BA
11Transparent pricing

Clear packages. No hidden fees.

Two service tiers based on how much support you need beyond the written report. Every case is personally reviewed and signed by Prof. İbrahim Yıldız.

Standard
Genomic Report

Complete fourteen-section written interpretation. For patients with a clear clinical trajectory seeking a definitive second read.

€2,000 EUR
  • 14-section structured IYGAS™ report
  • Variant interpretation & therapy matching
  • Active clinical trial recommendations
  • Patient-readable summary
  • 30-day email follow-up support
  • 3 business day delivery
Submit a case
12 · Built for two platforms

One platform
Three ways in

01 · For physicians

A clinical co-pilot, not a lab printout.

Workflow-integrated reports. EHR-compatible exports. Outcomes data. Direct line to the reviewing oncologist.

See physician workflow
ONCOLOGY · GU · GI · THORACIC · BREAST
02 · For patients & families

Why your doctor sent your report here.

We translate the genomic findings on your report into the treatment options your doctor will discuss with you—in plain language, with privacy protected.

Patient information →
PRIVATE · PHYSICIAN-REVIEWED · EXPLAINED
13Who we are

Expert-led. Technology-powered.

NGS Advisory is a boutique molecular oncology advisory — a small, specialized team combining deep clinical experience, cancer genomics expertise, and advanced technology.

İY

Prof. İbrahim Yıldız, MD

Medical Oncology · Clinical Lead

Professor of Medical Oncology at Acıbadem Mehmet Ali Aydınlar University, Istanbul. Member of ASCO and ESMO. Author of 130+ peer-reviewed publications. Personally reviews and signs every advisory.

AT

Assoc. Prof. Taşcı

Molecular Oncology · Genomics

Associate Professor specializing in cancer genomics, multi-platform NGS interpretation, and clinical trial matching. Leads the platform integration layer (DNA · RNA · protein · germline).

GC

Genomics Consultant

Molecular Biology & Cancer Genetics

Our genomics consultant is a specialist in cancer molecular biology with expertise in NGS data interpretation, variant annotation, and molecular pathway analysis. Their role is to ensure every genomic finding — from single nucleotide variants to complex structural rearrangements — is accurately characterized, correctly classified, and placed in the appropriate biological context.

Key responsibilities include multi-platform data integration (DNA + RNA + IHC), variant of unknown significance (VUS) biological assessment, clonal architecture interpretation, and quality control of genomic data accuracy. This layer of expertise ensures that the clinical recommendations built on top of the genomic data are based on correctly interpreted molecular findings — including cases where DNA and RNA results appear discordant and require careful biological explanation.

SE

Software Engineer

IYGAS™ Platform Architecture

The architect behind the Ibrahim Yildiz Genomic Advisory System™ (IYGAS) — the proprietary platform that structures, formats, scores, and produces our molecular advisory reports. The system integrates multi-platform NGS data, calculates immunotherapy suitability scores, generates tier classifications, and produces publication-quality formatted reports with color-coded clinical tables.

The IYGAS platform is not a generic template — it dynamically generates each report based on the individual patient’s genomic profile, tumor type, and available platform data. It incorporates real-time web verification of clinical trial statuses, FDA approval databases, and current NCCN guideline versions. The system enforces internal quality controls including VAF cross-referencing, platform-source tracking, and amber-field flagging for missing clinical data that must be completed by the treating physician.

14For patients & families

Questions we hear most.

Your NGS lab report is a technical document for molecular pathologists. It lists what was found but doesn't build a treatment strategy. Our advisory takes that same data and produces a complete clinical roadmap — prioritization, IO assessment, resistance planning, trial matching — that your treating oncologist can use directly.
We work with your existing report — no new testing required. We accept Tempus (xT, xR, RNA-Seq), FoundationOne CDx, Guardant360, Caris, and others. If your report includes multiple platforms (DNA + RNA + IHC), we integrate all of them.
No. Our report is a molecular advisory — a second opinion. All treatment decisions remain with your treating oncologist, who knows your full medical history and physical condition. Every report includes a clear statement that physician review is required before any clinical action.
The structured molecular advisory (IYGAS™) is always delivered in English — the international medical-genomics standard. The physician commentary is available in Turkish, English, Bulgarian, Romanian, and Bosnian, so your local oncologist receives a clear narrative in a language they're comfortable with.
01Physician-led clinical intelligence

Your NGS report decoded. Your treatment strategy refined.

A molecular second opinion in oncology. We turn complex genomic sequencing into clear, actionable clinical recommendations.

130+
Peer-reviewed publications
Prof. İbrahim Yıldız, MD
Phase 3
Principal Investigator
international trials
3 days
Median delivery
48–72 h priority
ASCO·ESMO
Active membership
guideline literacy
02How it works

From NGS upload to clinical advisory.

A streamlined, secure process for referring oncologists and patients seeking a molecular second opinion.

1
Step 01
Upload your NGS

Send your report (Tempus, FoundationOne, Guardant, Caris, or any panel) via our secure portal with basic clinical context.

2
Step 02
Multi-platform analysis

DNA · RNA · protein · IHC integrated, cross-referenced with current NCCN guidelines, FDA approvals, and active trials.

3
Step 03
Expert review

Prof. İbrahim Yıldız personally reviews every case, validating tier classifications, recommendations, and trial matches.

4
Step 04
Report delivery

Two documents within 48–72 h: the structured IYGAS™ advisory and the physician commentary. Optional video consult.

03What you get

Two documents.
One complete picture.

A structured English-language molecular advisory, plus a physician commentary in your preferred language.

IYGAS™ Molecular Advisory
14 SECTIONS
  • 02Executive clinical summary · critical findings
  • 05Auto-tier classification (IA → IV)
  • 06Treatment decision matrix (1L / 2L / 3L+)
  • 07Immunotherapy suitability score
  • 084-step resistance management strategy
  • 11Clinical trial matching framework
  • +…and 8 further sections, end to end
Physician Commentary
MULTILINGUAL
  • ·First-person clinical narrative by Prof. Yıldız
  • ·“Why this finding matters,” not just what it is
  • ·“Why I recommend this treatment”, with the evidence
  • ·IO score & VUS interpretation, in plain language
  • ·Available in TR · EN · BG · RO · BA
04Why a second opinion

Six layers beyond the standard report.

Standard NGS reports list mutations and mention drug matches. We add layers your treating oncologist can act on immediately.

01
Variant Tier Classification

Every variant graded Tier IA → IV per NCCN, OncoKB and FDA, then re-graded against your specific tumor type.

02
Immunotherapy Suitability Score

A quantitative IO score from five parameters: TMB · MSI · PD-L1 · driver penalty · ultra-low TMB penalty.

03
Treatment Sequencing 1L → 2L → 3L+

A sequence, not a single decision. Each line is annotated with ORR, PFS and OS evidence.

04
Anticipatory Resistance Strategy

What to test at progression, which resistance mutations to expect, and which next-gen agents address each.

İY
Prof. İbrahim Yıldız, MD
Medical Oncology · Clinical Lead

Professor of Medical Oncology at Acıbadem University, Istanbul. ASCO & ESMO member, author of 130+ peer-reviewed publications. Personally reviews and signs every advisory.

05Transparent pricing

Clear packages. No hidden fees.

Two tiers based on how much support you need beyond the written report. Every case is signed by Prof. Yıldız.

Standard
Genomic Report

Complete fourteen-section written interpretation, a definitive second read.

€2,000EUR
  • 14-section structured IYGAS™ report
  • Variant interpretation & therapy matching
  • Active clinical trial recommendations
  • 30-day email follow-up · 3-day delivery
Submit a case
RECOMMENDED
Premium
Report + Consultation

Everything in Standard, plus a 30-minute video consultation with Prof. Yıldız.

€2,750EUR
  • Everything in Standard
  • 30-min video consult w/ Prof. Yıldız
  • Priority turnaround in 48 hours
  • 60-day follow-up · EN·TR·BG·RO·BA
Submit a case
06For patients & families

Questions we hear most.

Your lab report is a technical document. It lists what was found but doesn’t build a strategy. We take that same data and produce a complete clinical roadmap: prioritization, IO assessment, resistance planning, trial matching.

We work with your existing report, no new testing required. We accept Tempus, FoundationOne CDx, Guardant360, Caris and others, and integrate multi-platform data (DNA + RNA + IHC).

No. Our report is a molecular advisory, a second opinion. All treatment decisions remain with your treating oncologist, who knows your full history. Physician review is required before any clinical action.

The structured IYGAS™ advisory is always in English, the international standard. The physician commentary is available in Turkish, English, Bulgarian, Romanian and Bosnian.

Begin a case

A molecular second opinion,
within days.

Upload your existing NGS report securely. Every case is personally reviewed and signed by Prof. İbrahim Yıldız.

Book a Consultation