MitoSuite: A Graphical Tool for Human Mitochondrial Genome Profiling in Massively Parallel Sequencing

Date : 01/01/2016 File : /Users/MitoSuite/preview.mapped_markdup.bam

Basic Profile

Summary Table

View table


Depth of Coverage

Zoom In: Dragging-area / Zoom Out: Right-clicking

Average Median Std. Q1 Q3 Max Min >10× >20× >30× >40× >50×
92.619 96.0 20.431 81.0 107.0 139.0 2.0 0.999 0.997 0.992 0.987 0.968

Depth table


Summary Statistics

Distribution Plot

* Mapping Quality (BinSize=5), Read Length (BinSize=5), GC-contents (BinSize=0.2)



Summary table


Avg.
Std.
Median Min Max Q1 Q3
MapQ 36.821 1.472 37.0 0.0 37.0 37.0 37.0
Length 70.333 20.323 71.0 30.0 94.0 52.0 93.0
GC(%) 44.575 6.637 44.595 22.892 73.333 40.0 48.936


Phred Score

Box Plot

* The blue box represents the interquantile range (IQR). The upper and lower whiskers show 1.5X IQR. The pink line represents the mean value.

Phred Score table

* Q1: 25th percentile, Q3: 75th percentile


ATGC Frequency

Line plot


Haplogroup Analysis

Estimated Haplogroups (PhyloTree Build 17)


Consensus Sequence

Sequence Support for assembly

The percentage of concordance across mitochondrial genome

Avg.
>0.5
>0.6
>0.7 >0.8 >0.9 =1.0
0.993 1.0 1.0 1.0 1.0 1.0 0.632

*The percentage of concordance represents consistent base per site of an assembled consensus sequence. Please see the support page for more information.

 consensus.fasta | * Unmapped sites , Phred Score <20 , and Concordance rate ≤0.5 are assigned to 'N' .

Substitutions vs. consensus sequence [Option : Detection of Heteroplasmic sites (MAF :0.05)]

Proportion of substitutions

*Substitution on all sites for an assembled consensus sequence.


Optinal Analysis

Disease-association Analysis (β)

Reports of Disease-Associations in MITOMAP(Oct 02, 2015 version).

*Position column shows a reference sequence position (rCRS).Mutation column means that of Allele in MITOMAP.Please check more detail information at MITOMAP.

Ancient DNA checker (β)

The percentage of mismatch bases on diagnostic sites

Avg.[%]
Std.
Median Min Max C.I.(95%)
1.08 1.394 0.877 0.0 5.31 0.71-1.45

*The percentage is based on inconsistent bases with polymorphic sites of an estimated haplogroup.


Deamination Check