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Table 1 Overview of CloVR analysis protocols

From: CloVR: A virtual machine for automated and portable sequence analysis from the desktop using cloud computing

Track

Process

Tool

Input

Output

CloVR-Search

Database search

BLAST [60]

nt or pep FASTA

BLAST output

CloVR-Microbe[38]

Assembly

Celera assembler [61], Velvet [51]

Raw sequence data (SFF, nt.FASTA1, nt.FASTQ1)

nt.FASTA

 

Gene prediction

Glimmer3 [62]

 

pep.FASTA

 

tRNA prediction

tRNA-scan [63]

 

GBK, SQN

 

rRNA prediction

RNAmmer [64]

 

GBK, SQN

 

Functional annotation

BLASTX against UniRef100 [58] and COG [65], HMMER [66] search against Pfam [67] and TIGRfam [68]

 

Annotated GBK, SQN

CloVR-16S

[39]

Quality checking

Mothur [17], Qiime [18]

nt.FASTA

nt.FASTA

 

Taxonomic classification

RDP classifier [69]

 

raw output, summary reports

 

Multiple sequence alignment

Mothur, Qiime (PyNAST)

 

nt.FASTA alignments

 

OTU clustering

Mothur (distance matrix), Qiime (uclust [70])

 

OTU list/table

 

α-diversity analysis

Mothur (collectors curves, rarefaction curves, diversity and richness estimators)

 

summary reports/diversity curves

 

β-diversity analysis

Metastats [71], custom R scripts, Qiime

 

summary reports/figures

CloVR-Metagenomics[40]

Clustering and artificial replicate removal

UCLUST

nt.FASTA

nt.FASTA

 

Functional classification

BLASTX against COG

 

raw output, summary reports

 

Taxonomic classification

BLASTN against RefSeq [72]

 

raw output, summary reports

 

Comparative analysis

Metastats, custom R scripts

 

summary reports/figures

  1. Abbreviations: nt, nucleotide; pep, peptide; GBK, GenBank.; SQN, Sequin (NCBI sequence submission table format);
  2. Key bioinformatics tools utilized in each protocol are listed. For input, only the required inputs from the user for each analysis track are listed. For outputs, only the data saved from each step is listed.
  3. 1- Inputs may require adapter and qc trimming prior to assembly