WGBS Depth Filter
Filter WGBS cytosine sites by a caller-supplied coverage depth.
Description
Bisulfite-sequencing depth is an upstream coverage criterion for interpreting a locus.
Bisulfite-sequencing depth is an upstream coverage criterion for interpreting a locus.1
Filter WGBS cytosine sites by a caller-supplied coverage depth.
When to use WGBS Depth Filter
Use this tool to filter WGBS cytosine sites by a caller-supplied coverage depth.
Prepare the already measured signals, counts, coordinates, fitted coefficients or sequence strings requested. Keep assay definitions, units, aligned lists and caller-selected thresholds consistent.
How to use WGBS Depth Filter and understand its results
- Prepare the already measured signals, counts, coordinates, fitted coefficients or sequence strings requested. Keep assay definitions, units, aligned lists and caller-selected thresholds consistent.
- Enter cytosineDepths, minimumDepth using the field table and calculation rules, then run the tool.
- Read passingIndexes, failedIndexes, passingPercent. The explanation below defines the units, signs, ordering and any flags or placeholder values.
- If the tool reports an input issue, correct the values and run it again. Apply the stated assumptions when interpreting a successfully returned result.
| Input field | Meaning | Value type; see rules below | Requirement |
|---|---|---|---|
| cytosineDepths | Cytosine depths | list of number | Required |
| minimumDepth | Minimum depth | number | Required |
Enter nonempty nonnegative integer depths and a nonnegative minimum. Return passing zero-based indices and percentage.
pass=depth≥minimum Units, indexing, boundary conditions and exceptional cases are defined in the calculation rules above.
| Output field | Meaning | Value type |
|---|---|---|
| passingIndexes | Passing indexes | list of number |
| failedIndexes | Failed indexes | list of number |
| passingPercent | Passing percent | number |
{
"input": {
"cytosineDepths": [
5,
10,
20
],
"minimumDepth": 10
},
"output": {
"passingIndexes": [
1,
2
],
"failedIndexes": [
0
],
"passingPercent": 66.66666666666666
}
} Limitations and assumptions
No alignment, methylation estimate or statistical precision is calculated.
Numeric inputs, where present, must be finite. Follow the calculation-specific rules for overflow, underflow and exceptional cases. Lists are limited to 100,000 entries; the rules above may require smaller limits. Missing required fields, extra fields, wrong value types and violations of the calculation rules are input errors.
Alternative or Complementary methods
Use Single-CpG Methylation: Calculate single-CpG methylation after background correction. For a complementary task, use RRBS Fragment Range: Filter RRBS fragment lengths against selected size bounds.
References
-
WGBS Depth Filter — tool.io
Similar or alternative tools
- Single-CpG Methylation
Calculate single-CpG methylation after background correction.
- RRBS Fragment Range
Filter RRBS fragment lengths against selected size bounds.