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![Page 1: Presentacion jbi](https://reader031.fdocuments.net/reader031/viewer/2022021813/5884cb061a28ab767c8b5071/html5/thumbnails/1.jpg)
Sample tracking using plasmid barcodes
Cristian Pérez GarcíaBioinformatician
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2© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
We regularly do clinical diagnosis
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3© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
ENAC Acreditation
Asked for:
- The ENAC acreditation of NextGeneDX (amplicon) analysis.
- The ENAC acreditation of clinical exome analysis
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4© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
But we had an Issue: sample traceability
• We until that moment did not traced back our samples from theVCF file to the DNA used for NGS.
• ENAC wisely asked to have biological sample tracking enabledin our lab (LIMS is not enough).
Resulting Genotype
Blood stock
DNA dilution
SequencingWet lab
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5© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
But we had an issue: sample traceability
• We until that moment did not traced back our samples from theVCF file to the DNA used for NGS.
• ENAC wisely asked to have biological sample tracking enabledin our lab (LIMS is not enough).
Resulting Genotype
Blood stock
DNA dilution
SequencingWet lab
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6© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Reasons to have a sample tracking system
Consequent to sample mix-ups in a research setting, erroneous data and sample matching may result in:
• Case-control: a loss of power for identification of causal variants.
• Clinical-context: This may lead to delayed or inaccurate reporting of results to patients.
Whilst good practice in the handling of samples and increased laboratory automation minimizes potential for error, additional checkpoints are still required to support quality control.
A method for post hoc confirmation of sample identity is therefore highly desirable.
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7© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Which options do we have?
• SNPs in Introns• Sequenom: ±24 SNPs in “pangenomic regions”.
• SNPs in Exons Capture• KASP: exonic SNPs in regions used
in capture methods
• Ampliseq
• STRs or indels
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8© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Are any of these suitable for us?
Which options do we have?
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9© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Choose SNPs in the region of the capture probes.
• SNPs in Introns• Sequenom: ±52 SNPs, some in introns.
• SNPs in Exons Capture• KASP: exonic SNPs in regions
used in capture methods
• Ampliseq
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10© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Choose SNPs in the region of the capture probes.
• SNPs in Introns• Sequenom: ±52 SNPs, some in introns
• SNPs in Exons Capture• KASP: exonic SNPs in regions
used in capture methods
• Ampliseq
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11© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
STRs or Indels
We don’t have a Sequenom, why don’t use STRs (SingleTandem Repeats) or indels and check with fragment lengthanalysis?
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12© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
STRs or Indels
We don’t have a Sequenom, why don’t use STRs (SingleTandem Repeats) or indels and check with fragment lengthanalysis?
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13© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
- Expensive
Disadvantages
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14© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
- Expensive
- Time Consuming
Disadvantages
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15© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
- Expensive
- Time Consuming
- Extra steps for our pipeline (genotyping)
Disadvantages
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16© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
• These are for tracking sample identity across multiple experiments.
Disadvantages
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17© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
• These are for tracking Sample identity across multiple experiments.
• This methods are not suitable for ampliconsequencing, without needing to do another genotyping step.
Disadvantages
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18© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Two weeks of thinkingand lots of coffee
breaks brain storming
But, is there a cheaper way to do this…?
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• Why not adding a sequence that is captured by the TSO?
• Nice idea, but....
• Should we need to use other approach with amplicons?
But, is there a cheaper way to do this…?
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20© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Let’s think again....
We have two workflows:
• Exoma capture
• Amplicons (Nextera after PCR)
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21© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Sample Tracking with Plasmids
• We can build a plasmid whoseinsert is a region of a genewith a probe in TruSight Oneand add some barcodes in themiddle of the sequence.
• PCR primers in both ends ofthe sequence.
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22© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Sample Tracking with Plasmids
• We can build a plasmid whoseinsert is a region of a genewith a probe in TruSight Oneand add some barcodes in themiddle of the sequence.
• PCR primers in both ends ofthe sequence.
This method should work for both workflows!
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23© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Selecting the region of interest
Find a captured region in TSO of not clinical interest with good capture
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• Which one to use?
• We are not reporting 3’-UTR miRNAtarget sites still has unclear diagnostic significance except for very specific cases.
Selecting the region of interest
TMEM-135 3’UTR (800x)
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Building the plasmid
• All tubes of NextGenDX ampliconswould have a sequence with NGSadapters so all tubes would reportthis barcode
• The barcode would be also captured and sequenced by TSO
STID:0204
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26© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Building the plasmid
CP-N701
acgtaccgtagaactagcgactgcCATTGGTGCCAGCTCTATAATTTCTTCTTCTTGTGGAATTAACAAAGAAAGGAGTGTCAAGGACTGAGATGACCCTCAGATTGGGGGGCTGTCTTAGATTCTAGGGCTTTGTAGTACTATGTTTCTGTTTAAAGTAGTGGCCTCAGGTGACTTTGTAATAGCCCTGTAGTTGCAAAAAGGTCGCCTTAGTAACTACAAAGAAATGAAACTGACTCTAGTGTGTGTGACTTCTGGAAACAGAAGTGGGGCAGTAAGTTGGCCATGATATAGCTAGTGTCATAGGACTACAGCAGAGTAGTGAGTGAATGGCCTTAAGCTTACAGCTGTGGTGAATAAGAATGTGTGCTATTTTACACACAGAAGAATggatcttcgattccatctgactgt
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27© 2016 IMEGEN – Información confidencial. Todos los derechos reservados.
Testing concentrations
Exome Amplicon
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Mapping and testing
[cpg@dream3 plasmidos]$ python3.4 checkPlasmids.py --folder 151209_NS500802_0062_AH5KF3AFXX-NxSqEx74/23732Mapping...# Searching for reads aligned with the plasmids referencesCP-N701 0CP-N702 1CP-N703 179CP-N704 115CP-N705 0CP-N706 0CP-N707 0CP-N710 0
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Results
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Amplicon test
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Exome test
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Expected results
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No plasmid added into sample
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Sample Swap
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35
Conclusions
• We have build a new, cheap and relatively simple technique for sample tracking.
• This technique does not require extra lab steps so that the protocol won’t take any longer.
• The sample tracking information is in the output data, so when evaluating the results, we can evaluate if sample swap has occurred.
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36© 2015 IMEGEN – Información confidencial. Todos los derechos reservados.
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Instituto de Medicina Genómica SLAgustín Escardino 9, Parc Científic de la Universitat de València46980 Paterna (Valencia, España)+34 963 212 340
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