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Base calling
Base calling is the process of assigning bases (nucleobases) to chromatogram peaks. One computer program for accomplishing this job is Phred base…
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Bioinformatics
Phred base calling
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
From sequence data to patient result: a solution for HIV drug resistance genotyping with Exatype, end to end software for Pol-HIV-1 Sequence analysis and patient HIV drug resistance result generation
Leonard Kingwara
,
M. Karanja
,
+7 authors
I. Mukui
2020
Corpus ID: 211226659
With the rapid scale-up of antiretroviral therapy (ART) to treat HIV infection, there are ongoing concerns regarding probable…
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2012
2012
Development of novel microsatellite markers for a specialist species of Lepidoptera, Boloria aquilonaris (Nymphalidae), based on 454 sequences
S. Vandewoestijne
,
C. Turlure
,
M. Baguette
2012
Corpus ID: 55643809
Microsatellites are the most common markers used in population and conservation genetic studies. However, their isola- tion is…
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2010
2010
A new approach for mutation analysis using data mining techniques
Hüseyin Kaya
,
Sule Gunduz Oguducu
International Conference on Computer Information…
2010
Corpus ID: 7431855
In this study, a new method is proposed to be used in diagnostic process of genetic disorders to determine the mutations in DNA…
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2008
2008
High throughput mitochondrial dna analysis. Optimization of sequence chemistry, characterization of local dye terminator sequencing frames, and tools for the development of an expert system
R. Roby
2008
Corpus ID: 83597286
Mitochondrial DNA (mtDNA) sequence analysis is a technique that is wellcharacterized, validated, and useful in the analysis of…
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2007
2007
Modelling along the DNA template in the Sanger method : inhibition through competition and form
D. Thornley
2007
Corpus ID: 14050326
DNA sequencing using the fluoresence based Sanger method comprises interpretation of a sequence of signal peaks of varying size…
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2006
2006
Technical Note GeneChip ® CustomSeq ® Resequencing Array Base Calling Algorithm Version 2 . 0 : Performance in Homozygous and Heterozygous SNP Detection
A. F F Y M E T R I X ® P R O D U C T F A
,
M. I. Ly > A
,
R. R. Ays A F F Y M E T R I X ® P R O D U C T F A
,
R. R. Ays
2006
Corpus ID: 534686
Large-scale comparative sequencing projects require a rapid, accurate, and cost-effective method for variant detection and…
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2006
2006
Trace modelling for abduction basecalling
D. Thornley
2006
Corpus ID: 14527482
DNA sequencing using the fluoresence based Sanger method comprises interpretation of a sequence of signal peaks of varying size…
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2005
2005
Accurate Base Calling from Multiple Electropherograms
Valerio Freschi
,
A. Bogliolo
2005
Corpus ID: 16174817
Introduction. DNA sequencing is an error-prone process composed of two main steps: generation of an electropherogram (or trace…
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2000
2000
Sequencing of β 2-Adreno-ceptor Gene PCR Products Using Taq BigDye Terminator Chemistry Results in Inaccurate Base Calling
R. Forrest
,
Huitong Zhou
,
J. Hickford
2000
Corpus ID: 3505405
2.Merril, C.R., D. Goldman, S.A. Sedman and M.H. Ebert. 1981. Ultrasensitive stain for proteins in polyacrylamide gels shows…
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2000
2000
Modelling electropherogram data for DNA sequencing using variable dimension MCMC
Nicholas M. Haan
,
S. Godsill
IEEE International Conference on Acoustics…
2000
Corpus ID: 18644599
DNA sequencing may be considered as a two stage process: the generation of noisy data indicative of DNA sequence by using…
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