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source_name:Genomic DNA for sample 04-018 Genomic DNA from 7 normal male individuals (Promega) title:04-018 gDNA, experiment ID 36320 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of large aberrations (Copy Number Variations). This particular array was used as the control as the native DNA pair for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification with an input of the same original gDNA.
source_name:Genomic DNA for sample 05-050 Genomic DNA from 7 normal male individuals (Promega) title:05-050 gDNA, experiment ID 42762 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of large aberrations (Copy Number Variations). This particular array was used as the control as the native DNA pair for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification with an input of the same original gDNA.
source_name:Genomic DNA for sample 04-018 title:04-018 vs. 04-018 gDNA (self), experiment ID 47750 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of large aberrations (Copy Number Variations). This particular array was accomplished to show the ratio of a DNA sample against itself on array, which was to demonstrate the variability/noise of the array hybridization itself. Theoretically the ratio should be 1 (or log2 ratio = 0).
source_name:5 ng of sample 05-050 genomic DNA, amplified using 40C-Wpa 5 ng genomic DNA from 7 normal male individuals (Promega), amplified using 40C-Wpa title:05-050 gDNA, 40C-Wpa, 5ng, experiment ID 94902 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of known large aberrations (Copy Number Variations). This particular array was applied for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification (40C-Wpa) with an input of the original gDNA.
source_name:5 ng of sample 04-018 genomic DNA, amplified using 40C-Wpa 5 ng genomic DNA from 7 normal male individuals (Promega), amplified using 40C-Wpa title:04-018 gDNA, 40C-Wpa, 5ng, experiment ID 98690 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of known large aberrations (Copy Number Variations). This particular array was applied for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification (40C-Wpa) with an input of the original gDNA.
source_name:5 ng of sample 05-050 genomic DNA, amplified using Wpa 5 ng genomic DNA from 7 normal male individuals (Promega), amplified using Wpa title:05-050 gDNA, Wpa, 5ng, experiment ID 141539 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of known large aberrations (Copy Number Variations). This particular array was applied for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification (Wpa) with an input of the original gDNA.
source_name:5 ng of sample 04-018 genomic DNA, amplified using Wpa 5 ng genomic DNA from 7 normal male individuals (Promega), amplified using Wpa title:04-018 gDNA, Wpa, 5ng, experiment ID 141542 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of known large aberrations (Copy Number Variations). This particular array was applied for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification (Wpa) with an input of the original gDNA.
source_name:0.1 ng of sample 04-018 genomic DNA, amplified using Wpa 0.1 ng genomic DNA from 7 normal male individuals (Promega), amplified using Wpa title:04-018 gDNA, Wpa, 0.1ng, experiment ID 141565 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of known large aberrations (Copy Number Variations). This particular array was applied for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification (Wpa) with an input of the original gDNA.
source_name:0.5 ng of sample 04-018 genomic DNA, amplified using Wpa 0.5 ng genomic DNA from 7 normal male individuals (Promega), amplified using Wpa title:04-018 gDNA, Wpa, 0.5ng, experiment ID 145381 description:HR-CGH was performed in order to demonstrate the detectability of the breakpoints and size of known large aberrations (Copy Number Variations). This particular array was applied for judging the possible locus-by-locus bias and distortion (if any) existed with the products resulted from the process of whole genome amplification (Wpa) with an input of the original gDNA.
[Oligo Array] Nimblegen WiCell HG18 WG CGH array (GPL7057)
genomic
Homo sapiens
unclassified
source_name:SOM01RYJ SOM01RYN title:NSCB_CGH_390K_H9.TSF_3618002.1 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V45 Human Reference Genomic DNA title:NSCB_CGH_390K_16236502 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V46 Human Reference Genomic DNA title:NSCB_CGH_390K_16236602 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V47 Human Reference Genomic DNA title:NSCB_CGH_390K_16246002 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V48 Human Reference Genomic DNA title:NSCB_CGH_390K_16250102 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V49 Human Reference Genomic DNA title:NSCB_CGH_390K_16250202 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V4E Human Reference Genomic DNA title:NSCB_CGH_390K_16250302 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V4J Human Reference Genomic DNA title:NSCB_CGH_390K_16250402 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.
[Oligo Array] WiCell HG18 WG CGH 385K v2 (GPL7717)
genomic
Homo sapiens
unclassified
source_name:SOM02V4G Human Reference Genomic DNA title:NSCB_CGH_390K_16250502 description:This CGH experiment is designed to detect deletion, insertation, amplication, etc. in the sample relative to the reference.