Free SCFHS Genomic & Biotechnology Technician mock test
25 original exam-style questions from our Genomic & Biotechnology Technician bank, timed at the exam’s own pace, scored against the 50% SCFHS pass mark. They span 6 of the 6 blueprint domains, so you will see exactly where you are weakest - free, no sign-up.
Sit 25 original exam-style questions at real exam pace
These are 25 original questions taken from our Genomic & Biotechnology Technician bank, spread across 6 of the 6 domains of the published blueprint. You get 72 seconds per question, which is exactly the pace of the real exam (30 minutes for 25). At the end you will see which domains you are weakest in, and the full worked reasoning for every question.
- 25
- questions
- 30:00
- time limit
- 50%
- SCFHS pass mark
A short diagnostic cannot predict whether you will pass - only the real exam does that. It will show you, honestly, where you currently stand.
Quick answer
The Genomic & Biotechnology Technician exam at a glance
The Genomic & Biotechnology Technician licensing exam is a computer-based, multiple-choice test, and each GCC regulator sets its own. SCFHS publishes exact figures, listed below. This free mock gives you 25 original exam-style questions at 72 seconds each, scored against the 50% SCFHS pass mark, then shows your weakest domains.
Published exam figures
- SCFHS
Saudi Classification Examination - Genomic and Biotechnology Technician
Saudi Arabia150 MCQs180 minutes50%
pass mark
- Attempts in the UAE
- 3 in total across DHA, DOH, MOHAP and SHA
- This free mock
- 25 questions · 30 minutes · 6 of 6 domains
- Full bank
- 450+ questions · 3 to 6 papers · AED 269
- Regulators
- SCFHS
How this free Genomic & Biotechnology Technician mock works
- 25
- original questions
- 30 min
- time limit
- 72s
- per question
- 6 of 6
- blueprint domains
- You get 72 seconds per question, the pace of a 150-question paper in 3 hours. The timer runs in your browser and ends the sitting when it reaches zero.
- Your score is set against the 50% SCFHS pass mark, the published figure for this exam. No other number is invented: there is no percentile and no pass probability.
- At the end you see your score, your pace per question, every domain ranked weakest first, and the worked answer and source for all 25 questions.
- You can mark each answer “sure” or “not sure”. Wrong answers you were sure about are shown first, because they are the ones you would not stop to check in the real exam.
- Your last result is saved in your own browser only, so you can come back and compare. Nothing is sent to us.
What the real Genomic & Biotechnology Technician licensing exam looks like
The Genomic & Biotechnology Technician exam is a computer-based multiple-choice paper, published by one regulator: SCFHS (pass mark 50%). Every regulator's format, pass mark and fee is in the table below; confirm yours before booking.
Pass marks at a glance: exam codes and pass marks by regulator for every written exam in one sourced table.
Before you can book the exam at all you need Dataflow primary source verification of your degree, licence and experience, which typically runs several weeks. Candidates often underestimate this and end up sitting the exam sooner after study than they planned. Check where you stand with our free eligibility checker or confirm whether your title even requires an exam using the Prometric exam checker.
You get three attempts in total across all UAE authorities, not three each, under the Unified Professional Qualification Requirements. At roughly AED 880 per attempt, plus the licensing delay each failure adds to your visa and start date, the cost of going in underprepared is not really the exam fee.
| Regulator | Exam | Format | Pass mark | Fee per attempt |
|---|---|---|---|---|
Saudi Classification Examination - Genomic and Biotechnology Technician | 150 MCQs in 180 minutes | 50% | Not published | |
No exam published for this title Not in the DHA CBT list; DHA's guideline assesses licensed titles that are not listed by oral | Not published | Not published | Not published | |
No exam published for this title DOH publishes no exam for this title that we could find; check with DOH | Not published | Not published | Not published | |
No exam published for this title MOHAP publishes no exam for this title that we could find; check with MOHAP | Not published | Not published | Not published | |
No exam published for this title SHA publishes no exam for this title that we could find; check with SHA | Not published | Not published | Not published | |
No exam published for this title No DHP Qatar exam blueprint published for this title; check with DHP | Not published | Not published | Not published | |
No exam published for this title NHRA publishes no exam for this title that we could find; check with NHRA | Not published | Not published | Not published | |
No exam published for this title No OMSB exam published for this title; check with OMSB | Not published | Not published | Not published | |
No exam published for this title Kuwait MOH publishes no exam for this title; check with the MOH | Not published | Not published | Not published |
Highlighted rows publish figures for this exact Genomic & Biotechnology Technician exam; the others show the regulator's general rules.
What is on the Genomic & Biotechnology Technician exam: the full blueprint
The published blueprint splits into 6 domains and 64 testable sub-topics. For each one you can see its weight, how many questions this mock asks on it, and about how many the full bank holds.
- Basic Laboratory Skills~14%
14 sub-topics · 4 in this mock · about 63 in the full bank
SCFHS Genomic and Biotechnology Technician examination content guideline V1.220901
- Molecular Techniques~17%
17 sub-topics · 4 in this mock · about 77 in the full bank
SCFHS Genomic and Biotechnology Technician examination content guideline V1.220901
- Biotechnology~29%
29 sub-topics · 7 in this mock · about 131 in the full bank
SCFHS Genomic and Biotechnology Technician examination content guideline V1.220901
- Genomics~17%
17 sub-topics · 5 in this mock · about 77 in the full bank
SCFHS Genomic and Biotechnology Technician examination content guideline V1.220901
- Bioinformatics~17%
17 sub-topics · 2 in this mock · about 77 in the full bank
SCFHS Genomic and Biotechnology Technician examination content guideline V1.220901
- Professional Practice/ Ethics~6%
6 sub-topics · 3 in this mock · about 27 in the full bank
SCFHS Genomic and Biotechnology Technician examination content guideline V1.220901
Bank counts are estimates from the published weights the bank is written to, rounded.
This mock samples 6 of 6 domains. The full bank covers all 6 across 450+ questions.
See the full bank - AED 269How to use your mock score
These bands are set against the 50% SCFHS pass mark and match the verdict on your result screen. On 25 questions, a score near the pass mark has a 95% margin of error of about ±20 points, so treat the band as a direction, not a forecast.
Below the line
On this sample you would likely fall short of the 50% pass mark today. Do not book yet. Start with your two weakest domains from the result, then sit full-length papers until you clear the line with room to spare.
Close to the line
A few questions decide it. On a 150-question paper, every 1% is one or two questions, so drill your weakest domains and build a margin on timed papers before you book.
On track
Clear of the pass mark on this sample. 25 questions is a small sample, so confirm it over full-length timed papers before you book: stamina and pacing fail candidates who know the material.
Getting an honest score
- 1Sit it cold, once. Do not look anything up. A diagnostic you help yourself through tells you nothing. The number you get is only useful if it is honest.
- 2Read every rationale, especially the ones you got right. Getting a question right by elimination is not the same as knowing it. The worked reasoning is free, whether or not you buy anything.
- 3Work on your weakest domain first. The breakdown orders your domains worst first for exactly this reason. Studying what you are already good at feels productive and moves nothing.
- 4Re-sit under full exam conditions later. The real paper is much longer than 25 questions and stamina matters. The full bank's 3 to 6 papers are written for exactly this.
A worked Genomic & Biotechnology Technician exam question
Every question in the mock and in the paid bank is written to this standard: a clinical stem, four plausible options and the reasoning for the answer, with its source.
Basic Laboratory Skills
A technician must prepare 500 mL of 0.5 M sodium chloride (molar mass 58.44 g/mol). How much NaCl should be weighed?
- A29.22 g
- B7.31 g
- C58.44 g
- D14.61 gCorrect
Why: Moles needed = 0.5 mol/L x 0.5 L = 0.25 mol, and 0.25 x 58.44 = 14.61 g. 29.22 g is for 1 litre, 7.31 g is for 250 mL, and 58.44 g is a full mole.
Source: Green and Sambrook, Molecular Cloning: A Laboratory Manual, 4th ed., 2012
Genomic & Biotechnology Technician sample questions with answers
10 more original exam-style Genomic & Biotechnology Technician questions, worked in full. They are not real or recalled exam questions, and none of them is in the mock above or on the bank page, so sit the mock first if you have not.
Question 1 · Basic Laboratory Skills
Human cell lines are handled at biosafety level 2. Why is a Class II biological safety cabinet preferred for this work?
- AHEPA-filtered airflow protects the operator, the cells and the environment
- BIt sterilises the work surface with ultraviolet light
- CIt removes chemical vapours by exhausting room air
- DIt maintains a constant 37 degree Celsius temperature for cell growth
Show answer and explanation
Correct answer: A. HEPA-filtered airflow protects the operator, the cells and the environment
Class II cabinets give inward airflow for the operator, HEPA-filtered downflow for the product and filtered exhaust for the environment. UV is only an adjunct, they do not protect against volatile chemicals, and they do not provide an incubator temperature.
Reference: CDC/NIH, Biosafety in Microbiological and Biomedical Laboratories, 6th ed., 2020
Question 2 · Biotechnology
A gene therapy design needs stable, long-term expression in dividing cells. Which vector choice fits best?
- AAn AAV vector, because it integrates at random in dividing cells
- BA lentiviral vector, because it integrates into the host genome
- CA naked plasmid, because it replicates forever in human cells
- DAn adenoviral vector, because it persists unchanged for years
Show answer and explanation
Correct answer: B. A lentiviral vector, because it integrates into the host genome
Lentiviral vectors integrate and so are passed on to daughter cells. AAV genomes stay mostly episomal and are diluted in dividing cells, plasmids are lost, and adenoviral genomes also remain episomal and are transient.
Reference: Gene and Cell Therapy: Biology and Applications, 1st ed., 2018
Question 3 · Biotechnology
Myeloma cells and B cells have been fused and are now grown in HAT medium. What does the medium achieve?
- AIt kills unfused B cells while the myeloma cells survive and grow
- BIt selects for cells that lack antibody genes
- CIt kills unfused myeloma cells, so that hybrids survive
- DIt stops the cells in the dish from dividing
Show answer and explanation
Correct answer: C. It kills unfused myeloma cells, so that hybrids survive
Myeloma partners lack HGPRT and cannot use the salvage pathway when aminopterin blocks the de novo pathway, while unfused B cells die naturally. Only hybrids survive.
Reference: Kohler and Milstein, Nature 1975;256:495-497
Question 4 · Bioinformatics
In a VCF file, a genotype field reads 0/1. What does it mean?
- AThe sample is homozygous for the reference allele at this position in both copies
- BThe sample is homozygous for the alternate allele at this position in both copies
- CThe sample is heterozygous: one reference and one alternate allele
- DThe genotype could not be called because of too few supporting reads
Show answer and explanation
Correct answer: C. The sample is heterozygous: one reference and one alternate allele
0/1 means one reference and one alternate allele. 0/0 is homozygous reference, 1/1 is homozygous alternate and ./. is a missing call.
Reference: Danecek et al., Bioinformatics 2011;27:2156-2158
Question 5 · Basic Laboratory Skills
A technician receives a new flammable solvent and is unsure how to store it safely. Which document gives product-specific storage, incompatibility and spill-response information?
- AThe manufacturer's safety data sheet for that exact product
- BThe product price list and ordering page in the supplier catalogue
- CThe label of a similar solvent already on the shelf
- DThe service manual of the fume hood
Show answer and explanation
Correct answer: A. The manufacturer's safety data sheet for that exact product
The safety data sheet is the standard source of hazards, storage, incompatibilities and spill response for a specific product. A price list has no safety content, a similar product may have different hazards, and a hood manual covers the equipment only.
Reference: United Nations, Globally Harmonized System of Classification and Labelling of Chemicals (GHS), 9th rev. ed., 2021
Question 6 · Biotechnology
A vector is cut with a single restriction enzyme and then treated with alkaline phosphatase before ligation with an insert. What is the purpose of the phosphatase step?
- AIt adds phosphate groups so that ligase works faster
- BIt removes 5' phosphates so the vector cannot re-close
- CIt cuts the insert at a second site to match the vector
- DIt destroys the restriction enzyme left in the tube
Show answer and explanation
Correct answer: B. It removes 5' phosphates so the vector cannot re-close
A vector cut at one site has compatible ends and can simply re-close. Removing its 5' phosphates blocks this because ligase needs them, while the insert still supplies phosphates. Phosphatase does not add phosphates, cut DNA or inactivate the restriction enzyme.
Reference: Green and Sambrook, Molecular Cloning: A Laboratory Manual, 4th ed., 2012
Question 7 · Genomics
A man with an X-linked recessive disorder has children with a woman who is not a carrier. What is the expected outcome?
- ASons are affected and daughters are unaffected non-carriers
- BHalf of the sons are affected and half of the daughters are carriers
- CDaughters are carriers and sons are unaffected
- DNeither sons nor daughters inherit the variant
Show answer and explanation
Correct answer: C. Daughters are carriers and sons are unaffected
A father passes his X chromosome to every daughter and his Y to every son. Daughters therefore carry the variant, and sons get a normal X from the mother. The other options describe a carrier mother or autosomal inheritance.
Reference: Strachan and Read, Human Molecular Genetics, 5th ed., 2018
Question 8 · Bioinformatics
After large FASTQ files are copied from the sequencer to a server, which check best shows that the copies are not corrupted?
- ACompare the file names and creation dates in the folder listing
- BOpen the first ten reads and read them by eye
- CCheck that the copy has the same file extension
- DCompare checksums, for example MD5, of the original and the copy
Show answer and explanation
Correct answer: D. Compare checksums, for example MD5, of the original and the copy
A checksum changes if even one bit differs, so matching values show the copy is identical. Names, dates and extensions can match while content is damaged, and viewing a few reads cannot detect corruption deeper in the file.
Reference: Buffalo, Bioinformatics Data Skills, 2015
Question 9 · Bioinformatics
FastQC shows base quality falling below Q20 in the last 20 positions of 150-base reads. Which step usually comes next?
- ADiscard the whole run and repeat the sequencing
- BConvert the FASTQ files to FASTA format so that the quality problem is removed
- CTrim the low-quality ends, and any adapter sequence, before alignment
- DAlign as they are, because aligners ignore base quality
Show answer and explanation
Correct answer: C. Trim the low-quality ends, and any adapter sequence, before alignment
Quality usually declines toward the 3' end, and trimming those bases keeps most of the data and avoids false mismatches. A run is rarely discarded for this, FASTA drops the quality information, and aligners do use base quality.
Reference: Bolger, Lohse and Usadel, Trimmomatic: a flexible trimmer for Illumina sequence data, Bioinformatics, 2014
Question 10 · Professional Practice/ Ethics
Exome sequencing for a child's epilepsy reveals a pathogenic variant in a hereditary cancer gene, unrelated to the test request. What should the technician do?
- ATelephone the parents directly to tell them about the finding
- BDelete the variant from the data because it is outside the request
- CAdd the variant to a shared research database for other groups
- DRecord it and refer it to the clinical geneticist
Show answer and explanation
Correct answer: D. Record it and refer it to the clinical geneticist
Unrequested findings are handled under the consent form and the laboratory's policy by the responsible clinical staff. A technician should not disclose results, delete data or share identifiable findings without consent.
Reference: Miller et al., ACMG recommendations for reporting of secondary findings in clinical exome and genome sequencing, v3.2, Genetics in Medicine, 2023
Free mock vs the full Genomic & Biotechnology Technician bank
The mock tells you where you stand. The bank is how you close the gap.
| What you get | Free mock | Full bank |
|---|---|---|
| Questions | 25 | 450+ |
| Papers | 1 short timed set | 3 to 6 full-length papers, about 150 each |
| Blueprint coverage | 6 of 6 domains | All 6 domains, 64 sub-topics |
| Worked rationale | Every question | Every question |
| Reference | Every question | Every question |
| Timing | 30 minutes in your browser | Exam-length papers to sit against the clock |
| Format | Online, free | PDF sent to you, yours to keep |
| Price | Free | AED 269, paid once |
Full Genomic & Biotechnology Technician bank
Close your gaps before exam day
- 450+ original questions in 3 to 6 full-length papers
- A worked rationale and a reference on every question
- Prepared for your regulator's blueprint and pass mark
One-time price
AED 269
About a third of one exam fee (about AED 880 per attempt)
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