Maverix Analytic Platform statistics

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Citations per year

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Popular tool citations

chevron_left Read alignment Bioinformatics workflows Novel transcript quantification Variant detection Depth of coverage chevron_right
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Tool usage distribution map

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Associated diseases

Associated diseases

Maverix Analytic Platform specifications


Unique identifier OMICS_04003
Name Maverix Analytic Platform
Software type Pipeline/Workflow
Interface Command line interface
Restrictions to use License purchase required
Biological technology Illumina, Life Technologies
Operating system Unix/Linux, Mac OS, Windows
Parallelization MapReduce
License Commercial
Computer skills Advanced
Stability No
High performance computing Yes
Maintained No


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Maverix Analytic Platform in publications

PMCID: 5892582
PMID: 29475944
DOI: 10.1074/jbc.RA117.001474

[…] strand-specific rna library prep kit (agilent technologies). multiplexed sequencing was run in a hiseq2500 sequencer (illumina). read alignment and gene expression levels were analyzed by the maverix analytic platform (maverix). the data set was culled from differentially expressed genes with a cutoff of at least a 2-fold change in expression levels (p value ≤0.05). the pathway enrichment […]

PMCID: 5192216
PMID: 28004802
DOI: 10.1038/ncomms13894

[…] manufacturer's protocol. cluster generation and 75 bp single read single-indexed sequencing was performed on illumina nextseq 500 (illumina). sequencing analysis was done using mrna-seq analysis on maverix analytic platform (maverix biomics, inc, san mateo, ca). raw sequencing reads from illumina sequencing platform that was converted into fastq file format were quality checked for potential […]

PMCID: 4815086
PMID: 27030474
DOI: 10.1186/s12864-016-2595-4

[…] tracks that contained genotypes of the cat trio were prepared for visualization and data comparison in the ucsc genome browser []. annotated variants were loaded into the variant database of the maverix analytic platform that included an interactive variant exploration tool for dynamic filtering of variants based on selected effects, quality scores, gene loci, and phenotypes. to verify […]

PMCID: 4637250
PMID: 26374066
DOI: 10.1111/age.12350

[…] genome wide and in the region of association and their depth of coverage were identified using dynamic filters based on phenotype‐specific allele frequencies in the variant explorer tool on the maverix analytic platform ( and viewed using the ucsc genome browser (rosenbloom et al. )., considering snp effects and their impacts (table s2), only five moderate impact variants […]

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