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This set of flashcards covers key concepts and terminology related to SNP filtering methodologies discussed in the lecture notes.
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SNP (Single Nucleotide Polymorphism)
A variation at a single position in a DNA sequence among individuals.
RAD-seq (Restriction site-associated DNA sequencing)
A cost-efficient method used for identifying SNPs by sequencing fragments around restriction enzyme cut sites.
Bioinformatics
The application of computer technology to manage and analyze biological data, particularly in genomics.
Artefact
An erroneous observation or result that is introduced during the experimental or analytical process.
Genotyping error
Mistakes in determining the genotype of an organism, often due to poor-quality data or inadequate methodologies.
Coverage effects
Variability in the representation of alleles in a sequencing run, often resulting from insufficient sequencing depth.
De novo assembly
The process of assembling sequences from scratch without a reference genome.
Library preparation
The process of preparing DNA fragments for sequencing, which includes steps like fragmentation, adapter ligation, and amplification.
PCR artefact
Errors related to polymerase chain reaction, such as chimeras or preferential amplification of certain fragments.
Linkage disequilibrium
Non-random association of alleles at different loci in a given population.
Quality control measures
Procedures implemented to ensure the quality and reliability of data collected during experiments.
Filtering strategies
Methods applied to data sets to remove low-quality data or artefacts to improve data reliability and accuracy.