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 |