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Table 1 Comprehensive table for comparison of the features of RFLP related software.

From: SNP-RFLPing: restriction enzyme mining for SNPs in genomes

 

Input format

Output format

Type of program

Flanking sequence length

Graphical display

Design of mutagenic primers

SNP-RFLPing

1.rs# IDs, ss# IDs.

2.Many IDs per line (separated by comma symbol).

3.HUGO gene name.

4.Entrez Gene ID.

5.SNP-in-sequences of IUPAC or [dNTP/dNTP] format.

6.Multiple mixed forms: rs#, ss# and sequences are accepted (separated by comma or enter key).

1.On-line and/or email.

2.SNP information provided, e.g., contig position, heterozygosity, function, protein codon.

3.RFLP information, e.g., recognition site, cutting position and strand of restriction enzyme. (visualization of the result).

4.Gene-SNP-RFLP function. (Users can input the gene name and the system can provide all RFLP SNPs of the gene)

Web-Server

User input

Yes

Yes

SNPicker [10]

1.sequences only.

1.RFLP information, e.g., recognition site, cutting position and strand of restriction enzyme.

2.no SNP information.

Down-load

User input

Yes

Yes

NEBcutter [1]

1.sequences only.

2.no SNP related input.

1.on-line only.

2.no SNP information.

Web-Server

User input

Yes

No

SRP Opt [11]

1.sequences only.

2.microbial genome only.

1.not for SNP genotyping.

2.selection of forensic markers.

Down-load

Not mentioned

Yes

No

PIRA-PCR Designer [12]

1.sequences only.

1.on-line only.

2.no SNP information.

Web-Server

User input

No

Yes

SNP cutter [13]

1.rs# IDs.

2.one ID per line.

3.Specific sequence format (additional software needed).

1.Email only.

2.no SNP information.

Web-Server

2000 bp

No

Yes

SNPselector [14]

1.upload input only.

2.rs# IDs.

3.gene name.

4.genome regions.

5.no sequence input.

1.Email only.

2.no RFLP information.

Web-Server

200 bp

Yes

No

SNP2CAPS [15]

1.alignment sequences.

2.FASTA format only.

1.no auto-mining for RFLP enzyme.

Down-load

Not mentioned

Yes

No

In silico software http://www.in-silico.com/restriction/ [16]

1.SNP ID.

2.sequences with SNP or mutation.

3.unaligned or multiple prealigned sequences are accepted.

1.on-line only.

2.SNP position in sequence.

3.RFLP information (including cutting position, selectable function for minimum recognition size, type of enzymes and commercial sources.).

4.multiple SNPs can be compared simultaneously.

5.other useful related tools provided.

Web-Server

User input

Yes

Yes