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Research data keyboard_double_arrow_right Dataset 2018figshare NSERC, CIHRSkinnider, Michael; Johnston, Chad; Nishanth Merwin; Dejong, Chris; Magarvey, Nathan;Complete set of 739 unique cyclodipeptide synthases identified in a global analysis of publicly available prokaryotic genomes. (XLSX 144Â kb)
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Research data keyboard_double_arrow_right Dataset 2017Figshare CIHRHaile, Simon; Corbett, Richard; MacLeod, Tina; Bilobram, Steve; Smailus, Duane; Tsao, Philip; Kirk, Heather; McDonald, Helen; Pandoh, Pawan; Bala, Miruna; Hirst, Martin; Miller, Diane; Moore, Richard; Mungall, Andrew; Schein, Jacquie; Coope, Robin; Yussanne Ma; Yongjun Zhao; Holt, Rob; Jones, Steven; Marra, Marco;Alignment-based metrics for reverse transcriptase comparisons. Table S2. Alignment-based metrics for the size selection experiment. Table S3. Alignment-based metrics for the comparison of library construction kits. Table S4. Alignment-based metrics for the intermediate ssRNA-seq pipeline. The protocol evaluated includes all changes (1st strand cDNA synthesis, optimal bead purifications, new library construction chemistry with modified ligation condition, bead-based size selection, and UNG treatment) with the exception of the mRNA isolation improvements. Table S5. Alignment-based metrics for the final ssRNA-seq pipeline using UHR. Table S6. Alignment-based metrics for the final ssRNA-seq pipeline using tumor samples. (XLS 62Â kb)
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Research data keyboard_double_arrow_right Dataset 2020figshare CIHRCastellani, Christina A.; Longchamps, Ryan J.; Sumpter, Jason A.; Newcomb, Charles E.; Lane, John A.; Grove, Megan L.; Bressler, Jan; Brody, Jennifer A.; Floyd, James S.; Bartz, Traci M.; Taylor, Kent D.; Penglong Wang; Tin, Adrienne; Coresh, Josef; Pankow, James S.; Fornage, Myriam; Guallar, Eliseo; O’Rourke, Brian; Pankratz, Nathan; Chunyu Liu; Levy, Daniel; Sotoodehnia, Nona; Boerwinkle, Eric; Arking, Dan E.;Additional file 4: Table S3. A. Results for 34 independent ARIC Discovery Meta-Analysis identified mtDNA-CN associated CpGs across all studied cohorts and Validation Meta-Analysis/All Cohort Meta-Analysis. Validation meta-analysis included CHS AA, CHS EA and FHS EA cohorts (P
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Research data keyboard_double_arrow_right Dataset 2018Wiley CIHRChen, Ying; Monaco, Simona; Crawford, Douglas J;Chen, Ying; Monaco, Simona; Crawford, Douglas J;Targets for goal-directed action can be encoded in allocentric coordinates (relative to another visual landmark), but it is not known how these are converted into egocentric commands for action. Here, we investigated this using a slow event-related fMRI paradigm, based on our previous behavioral finding that the Allocentric to Egocentric (Allo-Ego) conversion for reach is done at the first possible opportunity. Participants were asked to remember (and eventually reach toward) the location of a briefly presented target relative to another visual landmark. After a 1st memory delay, participants were forewarned by a verbal instruction if the landmark would reappear at the same location, (potentially allowing them to plan a reach following the auditory cue before the 2nd delay), or at a different location where they had to wait for the final landmark to be presented before response, and then reach toward the remembered target location. As predicted, participants showed landmark-centered directional selectivity in occipital-temporal cortex during the first memory delay, only developed egocentric directional selectivity in occipital-parietal cortex during the second delay for the “Same cue” task, and during response for the “Different cue” task. We then compared cortical activation between these two tasks at the times when the Allo-Ego conversion occurred, and found common activation in right precuneus, right pre-supplementary area and bilateral dorsal premotor cortex. These results confirm that the brain converts allocentric codes to egocentric plans at the first possible opportunity, and identify the four most likely candidate sites specific to the Allo-Ego transformation for reaches.
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Research data keyboard_double_arrow_right Dataset 2017Figshare CIHR, NIH | Core 3: Quantitative Prot... (1P01CA196539-01)Salloum, Ralph; McConechy, Melissa; Mikael, Leonie; Fuller, Christine; Drissi, Rachid; DeWire, Mariko; Nikbakht, Hamid; Jay, Nicolas De; Xiaodan Yang; Boue, Daniel; Chow, Lionel; Finlay, Jonathan; Tenzin Gayden; Karamchandani, Jason; Hummel, Trent; Olshefski, Randal; Osorio, Diana; Stevenson, Charles; Kleinman, Claudia; Majewski, Jacek; Fouladi, Maryam; Jabado, Nada;Copy number variation (CNV) segments in primary and recurrence tumors from 8 of 16 pairs of pHGG with matched normal tissue available. (XLSX 71Â kb)
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Research data keyboard_double_arrow_right Dataset 2017Figshare CIHRZahir, Farah; Mwenifumbo, Jill; Chun, Hye-Jung; Lim, Emilia; Karnebeek, Clara Van; Couse, Madeline; Mungall, Karen; Lee, Leora; Makela, Nancy; Linlea Armstrong; Boerkoel, Cornelius; Langlois, Sylvie; McGillivray, Barbara; Jones, Steven; Friedman, Jan; Marra, Marco;Test of relatedness - Table showing relatedness for each trio by comparing SNP concordance between child, mother and father. (XLSX 17 kb)
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Research data keyboard_double_arrow_right Dataset 2016Figshare CIHRTuor, Ursula; Zonghang Zhao; Barber, Philip; Qiao, Min;Tuor, Ursula; Zonghang Zhao; Barber, Philip; Qiao, Min;Additional file 4. Histological assessments for Figure 4. Shown are the data for each animal at either 1d or 3d post a single mild ischemic insult. Positive staining counts for TNF, Iba1 and EBA in addition to the Lectin scores and IgG gray level measures are presented.
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Research data keyboard_double_arrow_right Dataset 2019figshare CIHR, NIH | Strengthening the Integra... (5F31MH112397-02), NIH | Validation of Stigma Metr... (5R01MH110358-02)Kemp, Christopher; Jarrett, Brooke; Churl-Su Kwon; Lanxin Song; JettĂŠ, Nathalie; Sapag, Jaime; Bass, Judith; Murray, Laura; Rao, Deepa; Baral, Stefan;S1. Systematic review search strategy. Search terms, number of results, and filters used when collecting studies from databases for the systematic review. S2. Abstraction form and dataset. Abstraction form and dataset used for our analysis. (ZIP 148 kb)
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Research data keyboard_double_arrow_right Dataset 2016Figshare CIHR, NIH | Regulation of von Willebr... (5R21HL098672-02), NIH | Endothelial Activation an... (5R21HL129526-02)Graham, Susan; Junmei Chen; Chung, Dominic; Barker, Kevin; Conroy, Andrea; Hawkes, Michael; Namasopo, Sophie; Kain, Kevin; JosĂŠ LĂłpez; W. Liles;Additional file 2. Biomarkers for detailed sub-set analysis. This dataset was used for analysis of correlations of biomarkers at baseline and change in biomarkers from baseline to day 4. The file is available as an excel spreadsheet.
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Research data keyboard_double_arrow_right Dataset 2017Data Archiving and Networked Services (DANS) CIHRLee, J;Lee, J;Flow cytometric analyses of day 4 CD235a/Aldefluor and day20 MLC2V/CTNT expression of HES2 hESC (Figure S8) and MSC-iPS1 hiPSC lines (Figure S9)
Mendeley Data; EASY;... arrow_drop_down Mendeley Data; EASY; NARCISDataset . 2017add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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Research data keyboard_double_arrow_right Dataset 2018figshare NSERC, CIHRSkinnider, Michael; Johnston, Chad; Nishanth Merwin; Dejong, Chris; Magarvey, Nathan;Complete set of 739 unique cyclodipeptide synthases identified in a global analysis of publicly available prokaryotic genomes. (XLSX 144Â kb)
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Research data keyboard_double_arrow_right Dataset 2017Figshare CIHRHaile, Simon; Corbett, Richard; MacLeod, Tina; Bilobram, Steve; Smailus, Duane; Tsao, Philip; Kirk, Heather; McDonald, Helen; Pandoh, Pawan; Bala, Miruna; Hirst, Martin; Miller, Diane; Moore, Richard; Mungall, Andrew; Schein, Jacquie; Coope, Robin; Yussanne Ma; Yongjun Zhao; Holt, Rob; Jones, Steven; Marra, Marco;Alignment-based metrics for reverse transcriptase comparisons. Table S2. Alignment-based metrics for the size selection experiment. Table S3. Alignment-based metrics for the comparison of library construction kits. Table S4. Alignment-based metrics for the intermediate ssRNA-seq pipeline. The protocol evaluated includes all changes (1st strand cDNA synthesis, optimal bead purifications, new library construction chemistry with modified ligation condition, bead-based size selection, and UNG treatment) with the exception of the mRNA isolation improvements. Table S5. Alignment-based metrics for the final ssRNA-seq pipeline using UHR. Table S6. Alignment-based metrics for the final ssRNA-seq pipeline using tumor samples. (XLS 62Â kb)
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Research data keyboard_double_arrow_right Dataset 2020figshare CIHRCastellani, Christina A.; Longchamps, Ryan J.; Sumpter, Jason A.; Newcomb, Charles E.; Lane, John A.; Grove, Megan L.; Bressler, Jan; Brody, Jennifer A.; Floyd, James S.; Bartz, Traci M.; Taylor, Kent D.; Penglong Wang; Tin, Adrienne; Coresh, Josef; Pankow, James S.; Fornage, Myriam; Guallar, Eliseo; O’Rourke, Brian; Pankratz, Nathan; Chunyu Liu; Levy, Daniel; Sotoodehnia, Nona; Boerwinkle, Eric; Arking, Dan E.;Additional file 4: Table S3. A. Results for 34 independent ARIC Discovery Meta-Analysis identified mtDNA-CN associated CpGs across all studied cohorts and Validation Meta-Analysis/All Cohort Meta-Analysis. Validation meta-analysis included CHS AA, CHS EA and FHS EA cohorts (P
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Research data keyboard_double_arrow_right Dataset 2018Wiley CIHRChen, Ying; Monaco, Simona; Crawford, Douglas J;Chen, Ying; Monaco, Simona; Crawford, Douglas J;Targets for goal-directed action can be encoded in allocentric coordinates (relative to another visual landmark), but it is not known how these are converted into egocentric commands for action. Here, we investigated this using a slow event-related fMRI paradigm, based on our previous behavioral finding that the Allocentric to Egocentric (Allo-Ego) conversion for reach is done at the first possible opportunity. Participants were asked to remember (and eventually reach toward) the location of a briefly presented target relative to another visual landmark. After a 1st memory delay, participants were forewarned by a verbal instruction if the landmark would reappear at the same location, (potentially allowing them to plan a reach following the auditory cue before the 2nd delay), or at a different location where they had to wait for the final landmark to be presented before response, and then reach toward the remembered target location. As predicted, participants showed landmark-centered directional selectivity in occipital-temporal cortex during the first memory delay, only developed egocentric directional selectivity in occipital-parietal cortex during the second delay for the “Same cue” task, and during response for the “Different cue” task. We then compared cortical activation between these two tasks at the times when the Allo-Ego conversion occurred, and found common activation in right precuneus, right pre-supplementary area and bilateral dorsal premotor cortex. These results confirm that the brain converts allocentric codes to egocentric plans at the first possible opportunity, and identify the four most likely candidate sites specific to the Allo-Ego transformation for reaches.
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Research data keyboard_double_arrow_right Dataset 2017Figshare CIHR, NIH | Core 3: Quantitative Prot... (1P01CA196539-01)Salloum, Ralph; McConechy, Melissa; Mikael, Leonie; Fuller, Christine; Drissi, Rachid; DeWire, Mariko; Nikbakht, Hamid; Jay, Nicolas De; Xiaodan Yang; Boue, Daniel; Chow, Lionel; Finlay, Jonathan; Tenzin Gayden; Karamchandani, Jason; Hummel, Trent; Olshefski, Randal; Osorio, Diana; Stevenson, Charles; Kleinman, Claudia; Majewski, Jacek; Fouladi, Maryam; Jabado, Nada;Copy number variation (CNV) segments in primary and recurrence tumors from 8 of 16 pairs of pHGG with matched normal tissue available. (XLSX 71Â kb)
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Research data keyboard_double_arrow_right Dataset 2017Figshare CIHRZahir, Farah; Mwenifumbo, Jill; Chun, Hye-Jung; Lim, Emilia; Karnebeek, Clara Van; Couse, Madeline; Mungall, Karen; Lee, Leora; Makela, Nancy; Linlea Armstrong; Boerkoel, Cornelius; Langlois, Sylvie; McGillivray, Barbara; Jones, Steven; Friedman, Jan; Marra, Marco;Test of relatedness - Table showing relatedness for each trio by comparing SNP concordance between child, mother and father. (XLSX 17 kb)
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Research data keyboard_double_arrow_right Dataset 2016Figshare CIHRTuor, Ursula; Zonghang Zhao; Barber, Philip; Qiao, Min;Tuor, Ursula; Zonghang Zhao; Barber, Philip; Qiao, Min;Additional file 4. Histological assessments for Figure 4. Shown are the data for each animal at either 1d or 3d post a single mild ischemic insult. Positive staining counts for TNF, Iba1 and EBA in addition to the Lectin scores and IgG gray level measures are presented.
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Research data keyboard_double_arrow_right Dataset 2019figshare CIHR, NIH | Strengthening the Integra... (5F31MH112397-02), NIH | Validation of Stigma Metr... (5R01MH110358-02)Kemp, Christopher; Jarrett, Brooke; Churl-Su Kwon; Lanxin Song; JettĂŠ, Nathalie; Sapag, Jaime; Bass, Judith; Murray, Laura; Rao, Deepa; Baral, Stefan;S1. Systematic review search strategy. Search terms, number of results, and filters used when collecting studies from databases for the systematic review. S2. Abstraction form and dataset. Abstraction form and dataset used for our analysis. (ZIP 148 kb)
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Research data keyboard_double_arrow_right Dataset 2016Figshare CIHR, NIH | Regulation of von Willebr... (5R21HL098672-02), NIH | Endothelial Activation an... (5R21HL129526-02)Graham, Susan; Junmei Chen; Chung, Dominic; Barker, Kevin; Conroy, Andrea; Hawkes, Michael; Namasopo, Sophie; Kain, Kevin; JosĂŠ LĂłpez; W. Liles;Additional file 2. Biomarkers for detailed sub-set analysis. This dataset was used for analysis of correlations of biomarkers at baseline and change in biomarkers from baseline to day 4. The file is available as an excel spreadsheet.
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Research data keyboard_double_arrow_right Dataset 2017Data Archiving and Networked Services (DANS) CIHRLee, J;Lee, J;Flow cytometric analyses of day 4 CD235a/Aldefluor and day20 MLC2V/CTNT expression of HES2 hESC (Figure S8) and MSC-iPS1 hiPSC lines (Figure S9)
Mendeley Data; EASY;... arrow_drop_down Mendeley Data; EASY; NARCISDataset . 2017add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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