Bioinformatics Analyst

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Bioinformatics Analyst Interview Questions and Answers

Updated 2 Jun 2023

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Q1. What databases are used for population genetics

Ans.

Various databases are used for population genetics research, including dbSNP, 1000 Genomes Project, and HapMap.

  • dbSNP: a database of single nucleotide polymorphisms (SNPs) maintained by the National Center for Biotechnology Information (NCBI)

  • 1000 Genomes Project: a public database of genetic variation in over 2,500 individuals from 26 populations worldwide

  • HapMap: a database of common genetic variations in human populations, used to identify genetic factors associated with dise...read more

Q2. Which file formats are you familiar with

Ans.

I am familiar with various file formats used in bioinformatics.

  • FASTA

  • FASTQ

  • SAM/BAM

  • VCF

  • BED

  • GTF/GFF

  • WIG/BigWig

  • BAM/SAM

  • CRAM

  • BLAST

Q3. What databases are you familiar with

Ans.

I am familiar with various databases including GenBank, UniProt, NCBI, and PDB.

  • GenBank - a genetic sequence database maintained by NCBI

  • UniProt - a protein sequence and function database

  • NCBI - a collection of biomedical databases including GenBank and PubMed

  • PDB - a database of 3D structures of proteins and nucleic acids

Q4. Steps involved in NGS pipeline

Ans.

NGS pipeline involves steps like quality control, alignment, variant calling, annotation, and interpretation.

  • Quality control of raw data to remove low-quality reads and adapters

  • Alignment of reads to a reference genome or transcriptome

  • Variant calling to identify genetic variations

  • Annotation of variants to determine their functional impact

  • Interpretation of results to draw conclusions about the biological significance of the variants

  • Examples of tools used in NGS pipeline are Fas...read more

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Q5. Process of sequencing

Ans.

Sequencing is the process of determining the order of nucleotides in a DNA or RNA molecule.

  • DNA or RNA is extracted from the sample

  • The DNA or RNA is fragmented into smaller pieces

  • The fragments are amplified through PCR

  • The amplified fragments are sequenced using various methods such as Sanger sequencing or Next-Generation Sequencing (NGS)

  • The resulting sequence data is analyzed and assembled to generate the final sequence

Q6. Explain any NGS data analysis

Ans.

NGS data analysis involves processing and interpreting large amounts of sequencing data to extract meaningful biological insights.

  • NGS data analysis involves quality control, alignment, variant calling, and downstream analysis.

  • Tools like BWA, GATK, and SAMtools are commonly used for NGS data analysis.

  • Common analyses include identifying genetic variants, gene expression levels, and pathway analysis.

  • NGS data analysis can be used in genomics, transcriptomics, epigenomics, and met...read more

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Bioinformatics Analyst 0-1 years
Feathersoft Info Solutions Private Limited
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Bioinformatics Analyst 0-3 years
CRF - Chest Research Foundation
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