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Copy pathSequencingt empty dataframes.R
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Copy pathSequencingt empty dataframes.R
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76 lines (69 loc) · 2.43 KB
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# Illumina Short Read Sequencing
illumina_short_read_sequencing_df <- data.frame(
Well_Number_Well_Location = character(),
Sample_Name = character(),
Is_this_a_Human_Derived_Sample = character(),
SJ_Tissue_Bank = character(),
Sample_SJUID = character(),
Alternative_ID = character(),
Submission_Material = character(),
Xenograft = character(),
Application = character(),
Illumina_Sequencer = character(),
Run_Type = character(),
Read_Length = character(),
Molecules_Sequenced = character(),
Reference_Genome = character(),
Please_specify_Reference_Genome = character(),
User_Comments = character(),
stringsAsFactors = FALSE
)
# PacBio Long Read Sequencing
pacbio_long_read_sequencing_df <- data.frame(
Well_Number_Well_Location = character(),
Sample_Name = character(),
Is_this_a_Human_Derived_Sample = character(),
SJ_Tissue_Bank = character(),
Sample_SJUID = character(),
Alternative_ID = character(),
Application = character(),
Reference_Genome = character(),
User_Comments = character(),
Size_of_Amplicon_bp = character(),
Input_Material = character(),
Purification_Method = character(),
stringsAsFactors = FALSE
)
# Custom Genotyping (PowerPlex STR)
custom_genotyping_powerplex_str_df <- data.frame(
Well_Number_Well_Location = character(),
Sample_Name = character(),
Is_this_a_Human_Derived_Sample = character(),
SJ_Tissue_Bank = character(),
Sample_SJUID = character(),
Alternative_ID = character(),
User_Comments = character(),
Analysis = character(),
stringsAsFactors = FALSE
)
# Mapping and Methylation (CACT Genotyping)
mapping_methylation_cact_genotyping_df <- data.frame(
Well_Number_Well_Location = character(),
Sample_Name = character(),
Is_this_a_Human_Derived_Sample = character(),
SJ_Tissue_Bank = character(),
Sample_SJUID = character(),
Alternative_ID = character(),
Array = character(),
DNA_Sample_Type = character(),
stringsAsFactors = FALSE
)
# Print structure of each dataframe
cat("Illumina Short Read Sequencing columns:\n")
print(names(illumina_short_read_sequencing_df))
cat("\nPacBio Long Read Sequencing columns:\n")
print(names(pacbio_long_read_sequencing_df))
cat("\nCustom Genotyping (PowerPlex STR) columns:\n")
print(names(custom_genotyping_powerplex_str_df))
cat("\nMapping and Methylation (CACT Genotyping) columns:\n")
print(names(mapping_methylation_cact_genotyping_df))