Analyskod (Click to sort Ascending) | Beskriving (Click to sort Ascending) |
|---|---|
| MELLIFR010 | Metagenomic sequencing |
| MELLIFR020 | Metagenomic sequencing |
| MELLIFR030 | Metagenomic sequencing |
| MELNXTR010 | Metagenomic sequencing |
| MELNXTR020 | Metagenomic sequencing |
| MELNXTR030 | Metagenomic sequencing |
| MELPCFR010 | Metagenomic sequencing |
| MELPCFR020 | Metagenomic sequencing |
| MELPCFR030 | Metagenomic sequencing |
| METKAPR050 | Metagenomic sequencing. 50 M read pairs. |
| METLIFR010 | Metagenomic sequencing |
| METLIFR020 | Metagenomic sequencing |
| METLIFR030 | Metagenomic sequencing |
| METNXTR010 | Metagenomic sequencing |
| METNXTR020 | Metagenomic sequencing |
| METNXTR030 | Metagenomic sequencing |
| METPCFR010 | Metagenomic sequencing |
| METPCFR020 | Metagenomic sequencing |
| METPCFR030 | Metagenomic sequencing |
| METPCFR050 | Metagenomic sequencing |
| WGLLIFC030 | Whole-genome sequencing, large batch sizes, PE 2x150, 30x coverage, Low input PCR-free library preparation. Requires batch size of 48 or more. |
| WGLPCFC030 | Order of 49 or more samples. Whole genome sequencing, 30X coverage. TruSeq PCR free prep. |
| WGSKAPR020 | Whole genome sequencing, KAPA library prep, shallow sequencing for applications such as NIPT |
| WGSLIFC030 | Whole-genome sequencing, low input strategy. PE 2x150, 30x coverage |
| WGSLIFC060 | Whole genome sequencing. Low input strategy. 60 X coverage. 2 x 150 M paired reads |
| WGSLIFC090 | Whole-genome sequencing, PE 2x150, 90x coverage, PCR-free library preparation using low-input protocol |
| WGSPCFC030 | Whole genome sequencing, 30X coverage. TruSeq PCR free prep. |
| WGSPCFC060 | Whole genome sequencing, 60X coverage. TruSeq PCR free prep. |
| WGSPCFC090 | Whole genome sequencing, 90X coverage. TruSeq PCR free prep. |
| WGTLIFC030 | Whole genome sequencing of trio. Low input strategy. 30 X coverage |
| WGTPCFC030 | Trio/Family order. Whole genome sequencing, 30X coverage. TruSeq PCR free prep. |
| WGXCUSC000 | Rare Disease analysis of externally sequenced whole genome data. Delivery of results in Scout. |
| EXLKTTR020 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 20 M read pairs. |
| EXLKTTR040 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 40 M read pairs. |
| EXLKTTR060 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 60 M read pairs. |
| EXLKTTR080 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 80 M read pairs. |
| EXOKTTR020 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 20 M read pairs. |
| EXOKTTR030 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 30 M read pairs. |
| EXOKTTR040 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 40 M read pairs. |
| EXOKTTR060 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 60 M read pairs. |
| EXOKTTR080 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 80 M read pairs |
| EXOKTTR100 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 100 M read pairs. |
| EXOKTTR120 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 120 M read pairs. |
| EXOKTTR140 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 140 M read pairs. |
| EXTKTTR020 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 20 M read pairs. |
| EXTKTTR040 | Whole exome sequencing using Twist Biosciences core exome bait set and Kapa Hyper Plus library preparation, 40 M read pairs. |
| EXXCUSR000 | Rare Disease analysis of externally sequenced whole exome data. Delivery of results in Scout. |
| PALKTTR010 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 10 M read pairs. |
| PALKTTR020 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 20 M read pairs. |
| PALKTTR030 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 30 M read pairs. |
| PALKTTR040 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 40 M read pairs. |
| PALKTTR050 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 50 M read pairs. |
| PANKTTR010 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 10 M read pairs. |
| PANKTTR020 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 20 M read pairs. |
| PANKTTR030 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 30 M read pairs. |
| PANKTTR040 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 40 M read pairs. |
| PANKTTR050 | Panel-based sequencing using Twist Biosciences custom bait set and with Kapa Hyper Plus library preparation, 50 M read pairs. |
| RNAPOAR025 | RNA seq, poly-A based priming, 25 M read pairs, PE 2x150 bp using NovaSeq. |
| RNAPOAR030 | RNA seq, poly-A based priming, 30 M read pairs, PE 2x150 bp using NovaSeq |
| RNAPOAR050 | RNA seq, poly-A based priming, 50 M read pairs, PE 2x150 bp using NovaSeq. |
| RNAPOAR075 | RNA seq, poly-A based priming, 75 M read pairs, PE 2x150 bp using NovaSeq. |
| RNLPOAR025 | RNA seq, poly-A based priming, 25 M read pairs, PE 2x150 bp using NovaSeq, minimum 49 samples |
| RNLPOAR030 | RNA seq, poly-A based priming, 30 M read pairs, PE 2x150 bp using NovaSeq, minimum 49 samples. |
| RNLPOAR075 | RNA seq, poly-A based priming, 75 M read pairs, PE 2x150 bp using NovaSeq, minimum 49 samples. |
| RNXCUSR000 | Rare Disease analysis of externally sequenced RNA data. Delivery of results as agreed. |
| MWGNXTR003 | Microbial whole genome sequencing. 1-8 submitted samples. 3 M read pairs. |
| MWLNXTR002 | Microbial WGS, >=9 samples per submission. PE 2x100, Nextera prep. 2 M read pairs. |
| MWLNXTR003 | Microbial whole genome sequencing. 89-175 submitted samples. 3 M read pairs. |
| MWMNXTR002 | Microbial whole genome sequencing. Nextera prep. PE 2x100, 2 M read pairs |
| MWMNXTR003 | Microbial whole genome sequencing. 9-88 submitted samples. 3 M read pairs. |
| MWRNXTR003 | Microbial whole genome sequencing of routine samples. 3 M read pairs. Not available for all customers. |
| MWXNXTR002 | Microbial WGS, >176 samples per submission. PE 2x125, Modified Nextera prep. >50x coverage |
| MWXNXTR003 | Microbial whole genome sequencing. >175 submitted samples. 3 M read pairs. |
| VWGNXTK500 | Virus whole genome sequencing. Nextera sample prep. 2x100 sequencing. 0.5 M read pairs. |
| VWGNXTR001 | Viral whole genome sequencing (of amplicons). 1-48 submitted samples. 1 M read pairs. |
| VWLNXTR001 | Viral whole genome sequencing (of amplicons). >48 submitted samples. 1 M read pairs. |
| VWMNXTK500 | Virus whole genome sequencing >=24 samples. Nextera sample prep. 2x100 sequencing. 0.5 M read pairs. |
| RMLP10R300 | External prep. HiSeq2500 in rapid mode, ST 2x100 bp, 300 M read-pairs (2 lane) |
| RMLP10S130 | RML, NovaSeq S1, sequencing only, PE 2x100, 1300 M r-p |
| RMLP15R100 | RML, NovaSeq S4, sequencing only, PE 2x150, 100 M r-p |
| RMLP15R200 | RML, NovaSeq S4, sequencing only, PE 2x150, 200 M r-p |
| RMLP15R300 | RML, NovaSeq S4, sequencing only, PE 2x150, 300 M r-p |
| RMLP15R400 | RML, NovaSeq S4, sequencing only, PE 2x150, 400 M r-p |
| RMLP15R500 | RML, NovaSeq S4, sequencing only, PE 2x150, 500 M r-p |
| RMLP15R750 | RML, NovaSeq S4, sequencing only, PE 2x150, 750 M r-p |
| RMLP15R825 | RML, NovaSeq S4, sequencing only, PE 2x150, 825 M r-p |
| RMLP15S100 | RML, NovaSeq S4, sequencing only, PE 2x150, 1000 M r-p |
| RMLP15S125 | RML, NovaSeq S4, sequencing only, PE 2x150, 1250 M r-p |
| RMLP15S150 | RML, NovaSeq S4, sequencing only, PE 2x150, 1500 M r-p |
| RMLP15S175 | RML, NovaSeq S4, sequencing only, PE 2x150, 1750 M r-p |
| RMLS05R150 | External prep. HiSeq2500 in rapid mode, SR 1x50 bp, 150 M read-pairs (1 lane) |
| RMLS05R200 | RML, HiSeq 2500 high output, SR 1x50 cycles, 200 M r-p (one lane). Full flow cell must be ordered |