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I applied via Naukri.com and was interviewed in Jan 2023. There were 3 interview rounds.
I applied via Referral and was interviewed before Sep 2022. There were 2 interview rounds.
Variants are different forms or versions of something, often used in genetics to describe different versions of a gene.
Variants can refer to different versions of a gene or DNA sequence.
They can also refer to different versions of a product or software.
Interpreting a variant involves understanding its specific characteristics and implications.
In genetics, variants can be classified as benign, pathogenic, or of uncertai...
I applied via Indeed and was interviewed in Nov 2021. There were 3 interview rounds.
Datar Genetics interview questions for popular designations
Top trending discussions
I applied via LinkedIn and was interviewed in May 2022. There were 2 interview rounds.
I applied via Job Portal and was interviewed in Oct 2023. There was 1 interview round.
I applied via Recruitment Consulltant and was interviewed in Apr 2024. There were 3 interview rounds.
Basic aptitude test to check IQ level
posted on 20 Dec 2023
I applied via Recruitment Consulltant and was interviewed in Jul 2024. There were 5 interview rounds.
16 Year manager
For HIRA
Group discussion
posted on 14 Jun 2021
I applied via Walk-in and was interviewed in Dec 2020. There were 3 interview rounds.
NGS principles involve variant detection through sequencing and analysis of DNA or RNA samples.
NGS (Next Generation Sequencing) is a high-throughput technology used for DNA or RNA sequencing.
Variant detection involves identifying differences in DNA or RNA sequences compared to a reference genome.
NGS principles include library preparation, sequencing, and bioinformatics analysis.
Variant calling algorithms are used to id...
Variant calling is a process of identifying differences between a sample and a reference genome.
Variant calling is used in genomics to identify genetic variations that may be associated with disease or other traits.
It involves comparing a sample genome to a reference genome to identify differences, or variants, such as single nucleotide polymorphisms (SNPs) or insertions/deletions (indels).
Variant calling can be done u...
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Medgenome Labs
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