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Source code for tool_shed.galaxy_install.migrate.versions.0011_tools
"""
The following tools have been eliminated from the distribution:
1: Profile Annotations for a set of genomic intervals
2: Polymorphism of the Reads
3: Coverage of the Reads in wiggle format
4: Canonical Correlation Analysis
5: Convert Color Space to Nucleotides
6: Compute sequence length
7: Concatenate FASTA alignment by species
8: Filter sequences by length
9: FASTA-to-Tabular converter
10: FASTQSOLEXA-to-FASTA-QUAL extracts sequences and quality scores from FASTQSOLEXA data
11: Kernel Canonical Correlation Analysis
12: Kernel Principal Component Analysis
13: Format mapping data as UCSC custom track
14: Megablast compare short reads against htgs, nt, and wgs databases
15: Parse blast XML output
16: Principal Component Analysis
17: RMAP for Solexa Short Reads Alignment
18: RMAPQ for Solexa Short Reads Alignment with Quality Scores
19: Histogram of high quality score reads
20: Build base quality distribution
21: Select high quality segments
22: Tabular-to-FASTA
The tools are now available in the repositories respectively:
1: annotation_profiler
2: blat_coverage_report
3: blat_mapping
4: canonical_correlation_analysis
5: convert_solid_color2nuc
6: fasta_compute_length
7: fasta_concatenate_by_species
8: fasta_filter_by_length
9: fasta_to_tabular
10: fastqsolexa_to_fasta_qual
11: kernel_canonical_correlation_analysis
12: kernel_principal_component_analysis
13: mapping_to_ucsc
14: megablast_wrapper
15: megablast_xml_parser
16: principal_component_analysis
17: rmap
18: rmapq
19: short_reads_figure_high_quality_length
20: short_reads_figure_score
21: short_reads_trim_seq
22: tabular_to_fasta
from the main Galaxy tool shed at http://toolshed.g2.bx.psu.edu
and will be installed into your local Galaxy instance at the
location discussed above by running the following command.
"""
from __future__ import print_function