standalone version Search Results


fcs express standalone version 6 ruo  (KAUST Core Labs)
90
KAUST Core Labs fcs express standalone version 6 ruo
Fcs Express Standalone Version 6 Ruo, supplied by KAUST Core Labs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fcs express standalone version 6 ruo - by Bioz Stars, 2026-05
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source code, standalone versions, user manual, sample images, video tutorial and further documentation  (SourceForge net)
90
SourceForge net source code, standalone versions, user manual, sample images, video tutorial and further documentation
Source Code, Standalone Versions, User Manual, Sample Images, Video Tutorial And Further Documentation, supplied by SourceForge net, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
source code, standalone versions, user manual, sample images, video tutorial and further documentation - by Bioz Stars, 2026-05
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standalone version of mtoolbox  (SourceForge net)
90
SourceForge net standalone version of mtoolbox
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Standalone Version Of Mtoolbox, supplied by SourceForge net, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
standalone version of mtoolbox - by Bioz Stars, 2026-05
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ibex software standalone version  (Dropbox Inc)
90
Dropbox Inc ibex software standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Ibex Software Standalone Version, supplied by Dropbox Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/ibex software standalone version/product/Dropbox Inc
Average 90 stars, based on 1 article reviews
ibex software standalone version - by Bioz Stars, 2026-05
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primer premier 6 standalone version  (Premier Biosoft)
90
Premier Biosoft primer premier 6 standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Primer Premier 6 Standalone Version, supplied by Premier Biosoft, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primer premier 6 standalone version/product/Premier Biosoft
Average 90 stars, based on 1 article reviews
primer premier 6 standalone version - by Bioz Stars, 2026-05
90/100 stars
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standalone version  (KNIME GmbH)
90
KNIME GmbH standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Standalone Version, supplied by KNIME GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/standalone version/product/KNIME GmbH
Average 90 stars, based on 1 article reviews
standalone version - by Bioz Stars, 2026-05
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standalone version of gromacs  (Molecular Dynamics Inc)
90
Molecular Dynamics Inc standalone version of gromacs
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Standalone Version Of Gromacs, supplied by Molecular Dynamics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/standalone version of gromacs/product/Molecular Dynamics Inc
Average 90 stars, based on 1 article reviews
standalone version of gromacs - by Bioz Stars, 2026-05
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lhs unix library/standalone version  (Sandia National Laboratories)
90
Sandia National Laboratories lhs unix library/standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Lhs Unix Library/Standalone Version, supplied by Sandia National Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lhs unix library/standalone version/product/Sandia National Laboratories
Average 90 stars, based on 1 article reviews
lhs unix library/standalone version - by Bioz Stars, 2026-05
90/100 stars
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vina standalone version  (AUTODOCK GmbH)
90
AUTODOCK GmbH vina standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Vina Standalone Version, supplied by AUTODOCK GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vina standalone version/product/AUTODOCK GmbH
Average 90 stars, based on 1 article reviews
vina standalone version - by Bioz Stars, 2026-05
90/100 stars
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bttoxin_scanner standalone version  (Biotechnology Information)
90
Biotechnology Information bttoxin_scanner standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Bttoxin Scanner Standalone Version, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/bttoxin_scanner standalone version/product/Biotechnology Information
Average 90 stars, based on 1 article reviews
bttoxin_scanner standalone version - by Bioz Stars, 2026-05
90/100 stars
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standalone version of molegro virtual docker  (Molegro ApS)
90
Molegro ApS standalone version of molegro virtual docker
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Standalone Version Of Molegro Virtual Docker, supplied by Molegro ApS, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/standalone version of molegro virtual docker/product/Molegro ApS
Average 90 stars, based on 1 article reviews
standalone version of molegro virtual docker - by Bioz Stars, 2026-05
90/100 stars
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standalone version  (Biodesign International Inc)
90
Biodesign International Inc standalone version
a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in <t>MToolBox.</t> Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow
Standalone Version, supplied by Biodesign International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/standalone version/product/Biodesign International Inc
Average 90 stars, based on 1 article reviews
standalone version - by Bioz Stars, 2026-05
90/100 stars
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Image Search Results


a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in MToolBox. Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow

Journal: Human Genetics

Article Title: A multi-parametric workflow for the prioritization of mitochondrial DNA variants of clinical interest

doi: 10.1007/s00439-015-1615-9

Figure Lengend Snippet: a The histogram graphs the bimodal distribution of disease scores associated to 1872 non-synonymous variants (HmtDB, May 2014) observed in mtDNA sequences from healthy individuals and stored in HmtDB. The solid lines indicate the two gaussian components of the mixture model (McLachlan and Peel ) (46 and 54 %, respectively). The first component of the mixture model with the lowest disease score values included the most benign non-synonymous variants. The vertical dashed line is drawn at the selected Disease Score Threshold, DST, defined as 0.4311; non-synonymous variants featuring a DS above 0.4311 may, therefore, be considered potentially affecting function. b Box-plot diagram shows the disease scores of non-synonymous variants by class of ‘Neutral’ or ‘Disease’ prediction (disease scores ranging from 0.05 to 0.4311 and from 0.6565 to 0.9162, respectively, for each class) as returned by all six pathogenicity predictors implemented in MToolBox. Circles represent the outliers. c Empirical cumulative distribution function of nucleotide variability associated with the 816 non-synonymous variants, featuring a disease score above the established DST. Dashes vertical line indicates the nucleotide variability cutoff, NVC = 0.0026, defined as the third quartile of such distribution. Non-synonymous variants showing variability values below the NVC are filtered by the variant prioritization workflow

Article Snippet: Disease scores and prioritization criteria are now implemented in both the standalone version ( http://sourceforge.net/projects/mtoolbox/ ) as well as in the web version of MToolBox at MSeqDR portal ( https://mseqdr.org/mtoolbox.php ) (Falk et al. ).

Techniques: Variant Assay