Reputation: 13
I am trying to process a database of BLAST output to generate a data frame containing values for a given gene and given sample. When a gene is identified within a sample I would like the scaffold on which it was identified to be reported. If a given gene is NOT identified within a given sample I would like the cell to be filled with N/A.
sample_name scaffold gene_title match_(%)
P24_ST48 64 aadA12 94.56
401B_ST5223 381 blaTEM-163 99.65
P32_ST218 91 aadA24 90.41
HOS66_ST73 9 blaACT-5 72.31
HOS16_ST38 70 blaTEM-146 99.42
HOS56_ST131 48 aadA21 91.39
Ecoli_2009_1_ST131 41 sul1 99.88
PH152_ST95 37 dfrA33 83.94
Ecoli_2009_32_STNT 16 aac(3)-Ib 100.00
PH231_ST38 59 mph(D) 89.83
P44_STNT 135 blaTEM-105 99.88
Ecoli_2011_89_ST127 29 blaTEM-158 99.65
405C_ST1178 120 aadA1 99.75
P3_STNT 15 blaTEM-68 99.19
5A_ST34 174 blaTEM-127 99.88
P27_ST10 211 aph(3')-Ia 100.00
4D_ST767 393 blaTEM-152 98.95
P10_STNT 23 blaTEM-17 99.07
Ecoli_2014_27_ST131 49 sul2_15 99.88
Ecoli_2013_10_ST73 23 blaTEM-2 99.19
The output table would look something like:
Sample aadA1 aadA12 aadA24 blaTEM-163 ...
P24_ST48 N/A 64 N/A N/A
401B_ST5223 N/A N/A N/A 381
...
In excel I have concatenated the sample name and gene titles and reported the scaffold number on row where this string is identified using VLOOKUP - I have tried many different ways in R and am going around in circles.
Now trying to process +700 genes and +450 samples, the list of gene-sample combinations is getting somewhat laborious for excel to manage and I must find another solution with my collection of samples growing increasingly large.
Any help would be greatly appreciated.
Cheers,
Max
Upvotes: 0
Views: 57
Reputation: 887088
We can use dcast
from data.table
library(data.table)
dcast(setDT(df1), sample_name + match_... ~ gene_title, value.var = 'scaffold')
# sample_name match_... aac(3)-Ib aadA1 aadA12 ...
#1: 401B_ST5223 99.65 NA NA
#2: 405C_ST1178 99.75 NA 120
#3: 4D_ST767 98.95 NA NA
#4: 5A_ST34 99.88 NA NA
Upvotes: 0
Reputation: 16277
Here's how to do that with spread
from tidyr
library(tidyr)
df1%>%
spread(key = gene_title,value = scaffold)
sample_name match_... aac(3)-Ib aadA1 aadA12 ...
1 401B_ST5223 99.65 NA NA NA
2 405C_ST1178 99.75 NA 120 NA
3 4D_ST767 98.95 NA NA NA
4 5A_ST34 99.88 NA NA NA
5 Ecoli_2009_1_ST131 99.88 NA NA NA
...
Data
df1 <- read.table(text="sample_name scaffold gene_title match_(%)
P24_ST48 64 aadA12 94.56
401B_ST5223 381 blaTEM-163 99.65
P32_ST218 91 aadA24 90.41
HOS66_ST73 9 blaACT-5 72.31
HOS16_ST38 70 blaTEM-146 99.42
HOS56_ST131 48 aadA21 91.39
Ecoli_2009_1_ST131 41 sul1 99.88
PH152_ST95 37 dfrA33 83.94
Ecoli_2009_32_STNT 16 aac(3)-Ib 100.00
PH231_ST38 59 mph(D) 89.83
P44_STNT 135 blaTEM-105 99.88
Ecoli_2011_89_ST127 29 blaTEM-158 99.65
405C_ST1178 120 aadA1 99.75
P3_STNT 15 blaTEM-68 99.19
5A_ST34 174 blaTEM-127 99.88
P27_ST10 211 aph(3')-Ia 100.00
4D_ST767 393 blaTEM-152 98.95
P10_STNT 23 blaTEM-17 99.07
Ecoli_2014_27_ST131 49 sul2_15 99.88
Ecoli_2013_10_ST73 23 blaTEM-2 99.19",
header=TRUE,stringsAsFactors=FALSE)
Upvotes: 1