Annotates |
the depth & breadth of coverage of features from multiple files |
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1 |
bed to protein map |
genomic location of proteins for MVP |
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2 |
BED-to-bigBed |
converter |
Conversion
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2 |
BED-to-GFF |
converter |
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2 |
BED-to-GFF |
converter |
Conversion
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1 |
bed_clean |
clean up BED files |
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1 |
bed_closest |
find closest intervals |
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1 |
bed_collapse |
collapse intervals |
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1 |
bed_intersect |
intersect two interval sets |
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1 |
bed_overlap_significance |
significance of two interval sets overlapping |
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1 |
bed_resize |
change interval size |
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1 |
bed_shuffle |
shuffle intervals chromosome not weighted by length |
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1 |
bed_size_stat |
plot interval size distribution |
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1 |
bed_sort_with_header |
sort intervals with header lines |
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1 |
bed_to_bigwig |
make bigwig from BED or BAM |
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1 |
bed_window |
make a window around interval center |
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1 |
BedCov |
calculate read depth for a set of genomic intervals |
|
5 |
bedgraph-to-bigwig |
converter |
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1 |
BedToIntervalList |
convert coordinate data into picard interval list format |
|
14 |
bedtools AnnotateBed |
annotate coverage of features from multiple files |
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21 |
bedtools BAM to BED |
converter |
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23 |
bedtools BED to BAM |
converter |
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21 |
bedtools BED to IGV |
create batch script for taking IGV screenshots |
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16 |
bedtools BED12 to BED6 |
converter |
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20 |
bedtools BEDPE to BAM |
converter |
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21 |
bedtools ClosestBed |
find the closest, potentially non-overlapping interval |
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21 |
bedtools ClusterBed |
cluster overlapping/nearby intervals |
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20 |
bedtools ComplementBed |
Extract intervals not represented by an interval file |
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21 |
bedtools ExpandBed |
replicate lines based on lists of values in columns |
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20 |
bedtools FisherBed |
calculate Fisher statistic between two feature files |
|
20 |
bedtools FlankBed |
create new intervals from the flanks of existing intervals |
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21 |
bedtools Genome Coverage |
compute the coverage over an entire genome |
|
20 |
bedtools GroupByBed |
group by common cols and summarize other cols |
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20 |
bedtools JaccardBed |
calculate the distribution of relative distances between two files |
|
20 |
bedtools LinksBed |
create a HTML page of links to UCSC locations |
|
20 |
bedtools MakeWindowsBed |
make interval windows across a genome |
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21 |
bedtools MaskFastaBed |
use intervals to mask sequences from a FASTA file |
|
20 |
bedtools Merge BedGraph files |
combines coverage intervals from multiple BEDGRAPH files |
|
20 |
bedtools MergeBED |
combine overlapping/nearby intervals into a single interval |
|
20 |
bedtools MultiCovBed |
counts coverage from multiple BAMs at specific intervals |
|
20 |
bedtools Multiple Intersect |
identifies common intervals among multiple interval files |
|
23 |
bedtools OverlapBed |
computes the amount of overlap from two intervals |
|
20 |
bedtools RandomBed |
generate random intervals in a genome |
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21 |
bedtools ReldistBed |
calculate the distribution of relative distances |
|
20 |
bedtools ShuffleBed |
randomly redistrubute intervals in a genome |
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21 |
bedtools SlopBed |
adjust the size of intervals |
|
22 |
bedtools SortBED |
order the intervals |
|
20 |
bedtools SpacingBed |
reports the distances between features |
|
17 |
bedtools SubtractBed |
remove intervals based on overlaps |
|
20 |
bedtools TagBed |
tag BAM alignments based on overlaps with interval files |
|
20 |
bedtools WindowBed |
find overlapping intervals within a window around an interval |
|
20 |
bigWigToBedGraph |
Convert from bigWig to bedGraph format |
|
2 |
bowtie-to-bed |
converter |
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1 |
Cluster, infer trajectories and embed |
with scanpy |
|
7 |
Compute both the depth and breadth of coverage |
of features in file B on the features in file A (bedtools coverage) |
|
21 |
Concatenate |
two BED files |
Aggregation
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6 |
Convert BED to Feature Location Index |
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1 |
Convert BED to GFF |
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|
2 |
Convert from BAM to FastQ |
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|
13 |
Convert Genomic Intervals To BED |
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1 |
Convert Genomic Intervals To Strict BED |
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2 |
Convert Genomic Intervals To Strict BED12 |
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1 |
Convert Genomic Intervals To Strict BED6 |
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|
2 |
Convert GFF to BED |
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2 |
Convert gffCompare annotated GTF to BED |
for StringTie results |
|
4 |
Convert GTF to BED12 |
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1 |
Convert lped to plink pbed |
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2 |
Convert Picard Interval List to BED6 |
converter |
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2 |
Convert plink pbed to ld reduced format |
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2 |
Convert plink pbed to linkage lped |
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|
2 |
Count intervals in one file overlapping intervals in another file |
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2 |
Create a BedGraph of genome coverage |
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3 |
Create a histogram of genome coverage |
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|
3 |
CrossMap BED |
Convert genome coordinates or annotation files between genome assemblies |
|
5 |
Cytosine Report To Bedgraphs |
Converts genome-wide cytosine methylation report to Bedgraphs |
|
1 |
dNdS Report |
Calculate the dN/dS value for each region in a bed file |
|
2 |
Extract nucleotide range and flanking sequences |
Get FASTA sequences from BED interval |
|
1 |
extract-boxed-sequences |
Extracts boxed sequences from bed_input_file which has to be created with 'find-box', part of this utility |
|
2 |
extract_fastasequence |
using BED file |
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1 |
Fasta to Bed File |
Create Bed file from Multiple fasta file |
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1 |
fastSTRUCTURE. Step 1: BED, BIM and FAM file calculation |
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|
1 |
Filter BED on splice junctions |
that are not in a reference bed file |
|
1 |
filter-annotated-entries |
Split entries into two files based on whether they overlap annotations in a bed file |
|
2 |
Find Nested Alternate ORFs (nAlt-ORFs) |
from BED and 2bit/FASTA |
Coding region prediction
Codon usage analysis
Codon usage table generation
Genome annotation
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1 |
Gene BED To Exon/Intron/Codon BED |
expander |
|
1 |
Generate BED file |
for a list of genes |
|
1 |
GetFastaBed |
use intervals to extract sequences from a FASTA file |
|
20 |
GFF-to-BED |
converter |
|
2 |
GFF-to-BED |
converter |
Conversion
|
1 |
GraphEmbed |
Compute and plot a 2D embedding of a data matrix given supervised class information |
|
1 |
GTF-to-BEDGraph |
converter |
Conversion
|
1 |
homer_bed2pos |
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1 |
homer_pos2bed |
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1 |
idpEmbedder |
Embed human/mouse gene metadata into IDPicker files |
|
4 |
Intersect BAM alignments with intervals in another files |
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|
2 |
Intersect intervals |
find overlapping intervals in various ways |
|
22 |
LAV to BED |
Converts a LAV formatted file to BED format |
|
1 |
MACS2 bdgbroadcall |
Call broad peaks from bedGraph output |
|
9 |
MACS2 bdgcmp |
Deduct noise by comparing two signal tracks in bedGraph |
|
9 |
MACS2 bdgdiff |
Differential peak detection based on paired four bedgraph files |
|
10 |
MACS2 bdgpeakcall |
Call peaks from bedGraph output |
|
9 |
MAF to BED |
Converts a MAF formatted file to the BED format |
|
1 |
Map peptides to a bed file |
for viewing in a genome browser |
|
3 |
MapBed |
apply a function to a column for each overlapping interval |
|
21 |
mapper analyzer |
Read the output of an aligner, print statistics and possibly translate into BED or GBrowse formats. |
|
1 |
Merge BedGraph files |
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|
3 |
NucBed |
profile the nucleotide content of intervals in a FASTA file |
|
21 |
Nucleotide subsequence search |
providing regions in BED format |
|
2 |
proBAMconvert |
peptide identifications to proBAM or proBED |
|
1 |
QCEmbedder |
Attaches a table or an image to a given qc parameter. |
|
4 |
qiime2 diversity tsne |
t-distributed stochastic neighbor embedding |
|
2 |
Scanpy PlotEmbed |
visualise cell embeddings |
|
12 |
snp location to bed format |
convert SNP to interval |
|
1 |
Stitch Gene blocks |
given a set of coding exon intervals |
|
4 |
Translate BED Sequences |
3 frame translation of BED augmented with a sequence column |
|
1 |
Translate BED transcripts |
cDNA in 3frames or CDS |
|
1 |
VCF-BEDintersect: |
Intersect VCF and BED datasets |
|
5 |
vcf-to-bigwig |
converter |
|
1 |
VCFannotate: |
Intersect VCF records with BED annotations |
|
5 |
Wig/BedGraph-to-bigWig |
converter |
|
2 |