deepblue_flank {DeepBlueR} | R Documentation

## flank

### Description

Create a set of genomic regions that flank the query regions. The original regions are removed from the query. Use the merge command to combine flanking regions with the original query.

### Usage

    deepblue_flank(query_id = NULL, start = NULL, length = NULL,
      use_strand = NULL, user_key = deepblue_options("user_key"))

### Arguments

`query_id` | - A string (Query ID)
`start` | - A int (Number of base pairs after the end of the region. Use a negative number to denote the number of base pairs before the start of the region.)
`length` | - A int (The new region length)
`use_strand` | - A boolean (Use the region column STRAND to define the region direction)
`user_key` | - A string (users token key)

### Value

id - A string (id of the new query)

### See Also

Other Operating on the data regions: `deepblue_aggregate`, `deepblue_binning`, `deepblue_count_regions`, `deepblue_coverage`, `deepblue_distinct_column_values`, `deepblue_extend`, `deepblue_filter_regions`, `deepblue_get_experiments_by_query`, `deepblue_get_regions`, `deepblue_input_regions`, `deepblue_intersection`, `deepblue_merge_queries`, `deepblue_overlap`, `deepblue_query_cache`, `deepblue_query_experiment_type`, `deepblue_score_matrix`, `deepblue_select_annotations`, `deepblue_select_experiments`, `deepblue_select_regions`, `deepblue_tiling_regions`

### Examples

    annotation_id = deepblue_select_annotations(
        annotation_name="CpG Islands",
        genome="hg19", chromosome="chr1")
    deepblue_flank(query_id = annotation_id,
        start = 0, length = 2000,
        use_strand = TRUE)

[Package DeepBlueR version 1.14.0 Index]