|
|
| Name |
Description |
Version |
Minimum Galaxy Version |
|
|
data by a column and perform aggregate operation on other columns. |
2.1.1 |
16.01 |
|
|
data on any column using simple expressions |
1.1.0 |
16.01 |
|
|
Appends the average, min, max of datapoints per interval |
1.1.3 |
16.01 |
|
|
for any numerical column |
1.1.1 |
16.01 |
|
|
Pairwise Alignment Viewer |
1.0.0 |
16.01 |
|
|
for multiple columns |
1.0.0 |
16.01 |
|
|
of quality statistics |
1.0.0 |
16.01 |
|
|
significant single-SNP associations in case-control studies |
1.0.0 |
16.01 |
|
|
Convert from MasterVar to pgSnp format |
1.0.0 |
16.01 |
|
|
linkage disequilibrium and tag SNPs |
1.0.0 |
16.01 |
|
|
Convert from MasterVar to gd_snp table |
1.0.0 |
16.01 |
|
|
tools for functional profiling of gene lists |
1.0.0 |
16.01 |
|
|
significant single- and multi-locus SNP associations in case-control studies |
1.0.0 |
16.01 |
|
|
significant transcription factor binding sites from ChIP data |
1.0.0 |
16.01 |
|
|
functional annotation for a list of genes |
1.0.1 |
16.01 |
|
|
LASSO-Patternsearch algorithm |
1.0.0 |
16.01 |
|
|
Alignment coverage information |
1.0.1 |
16.01 |
|
|
given a set of genomic intervals |
1.0.1 |
16.01 |
|
|
Converts a MAF formatted file to FASTA format |
1.0.1 |
16.01 |
|
|
Converts a MAF formatted file to the BED format |
1.0.0 |
16.01 |
|
|
given a set of coding exon intervals |
1.0.1 |
16.01 |
|
|
given a set of genomic intervals |
1.0.1 |
16.01 |
|
|
by specified attributes |
1.0.1 |
16.01 |
|
|
by Size |
1.0.1 |
16.01 |
|
|
by Species |
1.0.0 |
16.01 |
|
|
Converts a MAF formatted file to the Interval format |
1.0.0 |
16.01 |
|
|
for display at UCSC |
1.0.0 |
16.01 |
|
|
by Species |
1.0.0 |
16.01 |
|
|
given a set of block numbers and a MAF file |
1.0.1 |
16.01 |
|
|
a MAF file |
1.0.1 |
16.01 |
|
|
by Species |
1.0.0 |
16.01 |
|
|
converts any FASTQ to Sanger |
1.0.0 |
16.01 |
|
|
converts between FASTQ data and other data formats |
1.0.0 |
16.01 |
|
|
SOLiD output to fastq |
1.0.0 |
16.01 |
|
|
converts SOLiD data to FASTQ data |
1.0.0 |
16.01 |
|
|
based on splicing profile. |
0.1.0 |
16.01 |
|
|
for Solexa file |
1.0.0 |
16.01 |
|
|
Converts an AXT formatted file to FASTA format |
1.0.0 |
16.01 |
|
|
of a file |
1.0.0 |
16.01 |
|
|
to an existing dataset |
1.0.0 |
16.01 |
|
|
Parse a UCSC Gene Table dump |
1.0.0 |
16.01 |
|
|
between two datasets |
1.0.0 |
16.01 |
|
|
delimiters to TAB |
1.0.0 |
16.01 |
|
|
of selected columns |
1.0.0 |
16.01 |
|
|
Converts a LAV formatted file to BED format |
1.0.0 |
16.01 |
|
|
expander |
1.0.0 |
16.01 |
|
|
side by side on a specified field |
2.0.2 |
16.01 |
|
|
two files side by side |
1.0.0 |
16.01 |
|
|
Converts an AXT formatted file to LAV format |
1.0.0 |
16.01 |
|
|
on a dataset |
0.0.1 |
16.01 |
|
|
tail-to-head |
1.0.0 |
16.01 |
|
|
leading or trailing characters |
0.0.1 |
16.01 |
|
|
columns from a table |
1.0.2 |
16.01 |
|
|
|
1.0.1 |
16.01 |
|
|
occurrences of each record |
1.0.2 |
16.01 |
|
|
expander |
1.0.0 |
16.01 |
|
|
two datasets a specific column of which has the same value |
1.0.0 |
16.01 |
|
|
from a file |
2.0.1 |
16.01 |
|
|
converter |
1.0.1 |
16.01 |
|
|
lines that match an expression |
1.0.1 |
16.01 |
|
|
to find common or distinct rows |
1.0.2 |
16.01 |
|
|
data in ascending or descending order |
1.0.3 |
16.01 |
|
|
as a new dataset |
1.0.0 |
16.01 |
|
|
a column from one Query against another Query |
1.0.0 |
16.01 |
|
|
lines from a dataset |
1.0.0 |
16.01 |
|
|
Converts an AXT formatted file to a concatenated FASTA alignment |
1.0.0 |
16.01 |
|
|
lines from a dataset |
1.0.0 |
16.01 |
|
|
of a dataset |
1.0.0 |
16.01 |
|
|
converter |
1.0.0 |
16.01 |
|
|
converter |
1.0.0 |
16.01 |
|
|
converter |
1.0.0 |
16.01 |
|
|
consecutive characters |
1.0.0 |
16.01 |
|
|
converter |
1.1.0 |
16.01 |
|
|
converter |
2.0.0 |
16.01 |
|
|
together |
1.0.1 |
16.01 |
|
|
using simple expressions |
0.1.1 |
16.01 |
|
|
from GFF data |
1.0.0 |
16.01 |
|
|
|
0.1 |
16.01 |
|
|
using simple expressions |
0.1.1 |
16.01 |
|
|
for SOLiD data |
1.0.0 |
16.01 |
|
|
|
1.0.0 |
16.01 |
|
|
for SOLiD data |
1.0.0 |
16.01 |
|
|
server |
1.0.1 |
16.01 |
|
|
Ensembl server |
1.0.1 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
Central server |
1.0.1 |
16.01 |
|
|
|
1.0.0 |
16.01 |
|
|
stored locally |
1.0.0 |
16.01 |
|
|
Human Hemoglobin Variants and Thalassemias |
2.0.0 |
16.01 |
|
|
creates a bed or xbed file containing from text query |
1.0.0 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
|
1.0.0 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
rice mart |
1.0.1 |
16.01 |
|
|
test server |
1.0.0 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
ENA SRA |
1.0.1 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
server |
1.0.1 |
16.01 |
|
|
server |
1.0.1 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
table browser |
1.0.0 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
table browser |
1.0.0 |
16.01 |
|
|
table browser |
1.0.0 |
16.01 |
|
|
server |
1.0.0 |
16.01 |
|
|
Test server |
1.0.1 |
16.01 |
|
|
(PSU prepared queries) |
1.0.0 |
16.01 |
|
|
HapMap Biomart |
0.0.01 |
16.01 |
|
|
reads mapping against reference sequence |
1.0.0 |
16.01 |
|
|
compare sequencing reads against UCSC genome builds |
1.0.0 |
16.01 |
|
|
reads mapping against reference sequence |
1.0.0 |
16.01 |
|
|
Prepare a dataset for the Velvet velvetg Assembler |
1.0.0 |
16.01 |
|
|
Velvet sequence assembler for very short reads |
1.0.0 |
16.01 |
|
|
- Multiple Em for Motif Elicitation |
1.0.0 |
16.01 |
|
|
from file browser |
0.0.1 |
16.01 |
|
|
from file browser (development) |
0.0.1 |
16.01 |
|
|
from file browser (test) |
0.0.1 |
16.01 |
|
|
- send data to GenomeSpace |
0.0.4 |
16.01 |
|
|
- receive data from GenomeSpace |
0.0.2 |
16.01 |
|
|
using coordinates from assembled/unassembled genomes |
2.2.3 |
16.01 |