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VWGDPTR001 Whole genome sequencing of SARS-CoV-2 amplicons. 1 M read pairs.
VWXONTR000 External Oxford Nanopore sequenced virus samples.
MWRNXTR003 Microbial whole genome sequencing. 3 M read pairs.
MWXNXTR003 Microbial whole genome sequencing. 3 M read pairs.
VWGNXTR001 Viral whole genome sequencing (of amplicons). 1 M read pairs.
RMLCUSR800 Ready Made Library, SP flowcell, custom recipe 800 M read pairs.
RMLCUSS160 Ready Made Library, S1 flowcell, custom recipe 1600 M read pairs.
RMLP05R800 Ready Made Library, SP flowcell, PE 2x50, 800 M read pairs.
RMLP15R020 Ready Made Library, PE 2x150, 20 M read pairs.
RMLP15R100 Ready Made Library, PE 2x150, 100 M read pairs.
RMLP15R200 Ready Made Library, PE 2x150, 200 M read pairs.
RMLP15R300 Ready Made Library, PE 2x150, 300 M read pairs.
RMLP15R400 Ready Made Library, PE 2x150, 400 M read pairs.
RMLP15R500 Ready Made Library, PE 2x150, 500 M read pairs.
RMLP15R750 Ready Made Library, PE 2x150, 750 M read pairs.
RMLP15S100 Ready Made Library, PE 2x150, 1000 M read pairs.
RMLP15S125 Ready Made Library, PE 2x150, 1250 M read pairs.
RMLP15S150 Ready Made Library, PE 2x150, 1500 M read pairs.
RMLP15S175 Ready Made Library, PE 2x150, 1750 M read pairs.
RMLP15S200 Ready Made Library, PE 2x150, 2000 M read pairs.
RMLP15S225 Ready Made Library, PE 2x150, 2250 M read pairs.
RMLP15S250 Ready Made Library, PE 2x150, 2500 M read pairs.
RMLP15S275 Ready Made Library, PE 2x150, 2750 M read pairs.
RMLP15S300 Ready Made Library, PE 2x150, 3000 M read pairs.
RMLP15S325 Ready Made Library, PE 2x150, 3250 M read pairs.
RMLP15S350 Ready Made Library, PE 2x150, 3500 M read pairs.
RMLP15S375 Ready Made Library, PE 2x150, 3750 M read pairs.
RMLP15S400 Ready Made Library, PE 2x150, 4000 M read pairs.
RMLP15S425 Ready Made Library, PE 2x150, 4250 M read pairs.
RMLP15S450 Ready Made Library, PE 2x150, 4500 M read pairs.
RMLP15S475 Ready Made Library, PE 2x150, 4750 M read pairs.
RMLP15S500 Ready Made Library, PE 2x150, 5000 M read pairs.
PANKTTR020 Panel-based sequencing, 20 M read pairs.
PANKTTR040 Panel-based sequencing, 40 M read pairs.
PANKTTR060 Panel-based sequencing, 60 M read pairs.
PANKTTR080 Panel-based sequencing, 80 M read pairs.
PANKTTR100 Panel-based sequencing, 100 M read pairs.
PANKTTR200 Panel-based sequencing, 200 M read pairs.
PANWTTR020 Panel-based sequencing using Watchmaker Genomics library prep kit and Twist Biosciences custom bait set, 20 M read pairs. Only for in-house use.
PAZKTTR020 Panel-based sequencing, 20 M read pairs. No specified percent reads guaranteed. Only possible to order for specific customers.
PAZKTTR060 Panel-based sequencing, 60 M read pairs. No specified percent reads guaranteed. Only possible to order for specific customers.
PAZKTTR100 Panel-based sequencing, 100 M read pairs. No specified percent reads guaranteed. Only possible to order for specific customers.
EXOKTTR040 Whole exome sequencing, 40 M read pairs.
EXOKTTR060 Whole exome sequencing, 60 M read pairs.
EXOKTTR100 Whole exome sequencing, 100 M read pairs.
EXOKTTR140 Whole exome sequencing, 140 M read pairs.
EXOKTTR200 Whole exome sequencing, 200 M read pairs.
EXXCUSR000 Analysis of externally sequenced whole exome data.
METLIFR030 Metagenomic sequencing, low input PCR-free library preparation, 30 M read pairs.
METPCFR030 Metagenomic sequencing, 30 M read pairs.
METPCFR050 Metagenomic sequencing, 50 M read pairs.
WGSDPFR020 For internal use only
WGSDPFR140 For internal use only
WGSDPFR400 Whole genome sequencing, Illumina DNA Prep PCR free.
WGSLIFC030 Whole-genome sequencing, low input PCR-free library preparation, 30x coverage.
WGSLIFR400 Whole-genome sequencing, low input PCR-free library preparation, 400 M read pairs.
WGSLIFR500 Whole-genome sequencing, low input PCR-free library preparation. This application tag should only be used when the source of DNA is muscle. 500 M read pairs.
WGSLIFS120 Whole-genome sequencing, low input PCR-free library preparation, 1200 M read pairs.
WGSPCFC030 Whole genome sequencing. 30x coverage.
WGSPCFR010 Whole genome sequencing, 10 M read pairs. Only for in-house use.
WGSPCFR400 Whole-genome sequencing, 400 M read pairs.
WGSPCFR500 Whole-genome sequencing. This application tag should only be used when the source of DNA is muscle. 500 M read pairs.
WGSPCFS120 Whole-genome sequencing, 1200 M read pairs.
WGSWPFR020 Whole-genome sequencing with Watchmaker genomics PCR-free prep, PE 2x150bp, 20 M r-p. Only for in-house use.
WGSWPFR400 Whole-genome sequencing, Watchmaker genomics PCR-free prep, 400 M read pairs. Only for in-house use.
WGXCUSC000 Analysis of externally sequenced whole genome data.
RNADEPR050 RNA sequencing, rRNA depletion, 50 M read pairs.
RNADEPR100 RNA sequencing, rRNA depletion, 100 M read pairs.
RNAPOAR050 RNA sequencing, poly-A capture, 50 M read pairs.
RNAPOAR100 RNA sequencing, poly-A capture, 100 M read pairs.
RNAPOAR400 RNA sequencing, poly-A capture, 400 M read pairs.
RNXCUSR000 Analysis of externally sequenced RNA data.

WGSLIFS120

Whole-genome sequencing, low input PCR-free library preparation, 1200 M read pairs. wgs

Ackreditering ISO/IEC 17025:2017
Svarstid 21 dagar
Min. order 1 prov
Sekvensdjup
Provmängd 400 ng
Prioritetsalternativ Ja

Details

Whole-genome sequencing, low input PCR-free library preparation. Paired end 2x150 bp using NovaSeq X, 75% of ordered quantity of data guaranteed. Not compatible with FFPE material. Somatic analyses (Balsamic) of samples are not accredited.

Limitations

Whole genome sequencing does not provide a complete coverage of the human genome due to certain regions being difficult to accurately represent in sequence data. No specific coverage is guaranteed, only a certain number of reads. Individual samples may have a better or poorer performance, which should be considered in the interpretation of the results.

Last updated: Mon Nov 27 2023