SRX23868376 GM12878-NA-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687244 GM12878-NA-1 GM12878-NA-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868377 GM12878-low_APH-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687267 GM12878-low_APH-1 GM12878-low_APH-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868378 GM12878-low_APH-RO3306-release-M-high_APH_M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687246 GM12878-low_APH-RO3306-release-M-high_APH_M-1 GM12878-low_APH-RO3306-release-M-high_APH_M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868379 HCT116-low_APH-RO3306-release-M-POLQ-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687247 HCT116-low_APH-RO3306-release-M-POLQ-NU7441-1 HCT116-low_APH-RO3306-release-M-POLQ-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868380 HCT116-low_APH-RO3306-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687277 HCT116-low_APH-RO3306-G2-1 HCT116-low_APH-RO3306-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868381 HCT116-RO3306-release-M-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687273 HCT116-RO3306-release-M-2 HCT116-RO3306-release-M-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868382 HCT116-RO3306-release-M-high_APH_M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687274 HCT116-RO3306-release-M-high_APH_M-1 HCT116-RO3306-release-M-high_APH_M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868383 GM12878-low_APH-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687278 GM12878-low_APH-ART558-1 GM12878-low_APH-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868384 HCT116-low_APH-RO3306-release-M-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687252 HCT116-low_APH-RO3306-release-M-2 HCT116-low_APH-RO3306-release-M-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868385 HCT116-low_APH-RO3306-release-M-high_APH_M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687255 HCT116-low_APH-RO3306-release-M-high_APH_M-1 HCT116-low_APH-RO3306-release-M-high_APH_M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868386 HCT116-NA-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687271 HCT116-NA-1 HCT116-NA-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868387 HCT116-low_APH-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687254 HCT116-low_APH-1 HCT116-low_APH-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868388 HCT116-RO3306-G2-5 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687256 HCT116-RO3306-G2-5 HCT116-RO3306-G2-5 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868389 HCT116-low_APH-RO3306-G2-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687259 HCT116-low_APH-RO3306-G2-4 HCT116-low_APH-RO3306-G2-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868390 HCT116-RO3306-G2-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687284 HCT116-RO3306-G2-ART558-1 HCT116-RO3306-G2-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868391 HCT116-low_APH-RO3306-G2-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687263 HCT116-low_APH-RO3306-G2-ART558-1 HCT116-low_APH-RO3306-G2-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868392 HCT116-RO3306-release-M-6 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687265 HCT116-RO3306-release-M-6 HCT116-RO3306-release-M-6 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868393 HCT116-low_APH-RO3306-release-M-6 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687264 HCT116-low_APH-RO3306-release-M-6 HCT116-low_APH-RO3306-release-M-6 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868394 GM12878-low_APH-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687266 GM12878-low_APH-NU7441-1 GM12878-low_APH-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868395 HCT116-RO3306-release-M-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687268 HCT116-RO3306-release-M-ART558-1 HCT116-RO3306-release-M-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868396 HCT116-low_APH-RO3306-release-M-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687300 HCT116-low_APH-RO3306-release-M-ART558-1 HCT116-low_APH-RO3306-release-M-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868397 HCT116-RO3306-G2-6 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687292 HCT116-RO3306-G2-6 HCT116-RO3306-G2-6 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868398 HCT116-low_APH-RO3306-G2-5 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687295 HCT116-low_APH-RO3306-G2-5 HCT116-low_APH-RO3306-G2-5 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868399 HCT116-RO3306-G2-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687291 HCT116-RO3306-G2-ART558-2 HCT116-RO3306-G2-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868400 HCT116-low_APH-RO3306-G2-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687270 HCT116-low_APH-RO3306-G2-ART558-2 HCT116-low_APH-RO3306-G2-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868401 HCT116-RO3306-release-M-7 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687290 HCT116-RO3306-release-M-7 HCT116-RO3306-release-M-7 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868402 HCT116-low_APH-RO3306-release-M-7 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687269 HCT116-low_APH-RO3306-release-M-7 HCT116-low_APH-RO3306-release-M-7 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868403 HCT116-RO3306-release-M-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687299 HCT116-RO3306-release-M-ART558-2 HCT116-RO3306-release-M-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868404 HCT116-low_APH-RO3306-release-M-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687272 HCT116-low_APH-RO3306-release-M-ART558-2 HCT116-low_APH-RO3306-release-M-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868405 GM12878-low_APH-ART558-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687275 GM12878-low_APH-ART558-NU7441-1 GM12878-low_APH-ART558-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868406 HCT116-low_APH-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687309 HCT116-low_APH-2 HCT116-low_APH-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868407 HCT116-low_APH-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687303 HCT116-low_APH-ART558-1 HCT116-low_APH-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868408 HCT116-low_APH-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687276 HCT116-low_APH-NU7441-1 HCT116-low_APH-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868409 HCT116-low_APH-ART558-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687279 HCT116-low_APH-ART558-NU7441-1 HCT116-low_APH-ART558-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868410 HCT116-RO3306-release-M-9 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687304 HCT116-RO3306-release-M-9 HCT116-RO3306-release-M-9 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868411 HCT116-low_APH-RO3306-release-M-10 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687280 HCT116-low_APH-RO3306-release-M-10 HCT116-low_APH-RO3306-release-M-10 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868412 HCT116-low_APH-RO3306-release-M-ART558-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687310 HCT116-low_APH-RO3306-release-M-ART558-3 HCT116-low_APH-RO3306-release-M-ART558-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868413 HCT116-low_APH-RO3306-release-M-NVB-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687281 HCT116-low_APH-RO3306-release-M-NVB-2 HCT116-low_APH-RO3306-release-M-NVB-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868414 HCT116-S-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687282 HCT116-S-1 HCT116-S-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868415 HCT116-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687283 HCT116-G2-1 HCT116-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868416 GM12878-RO3306-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687301 GM12878-RO3306-G2-1 GM12878-RO3306-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868417 HCT116-M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687285 HCT116-M-1 HCT116-M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868418 HCT116-low_APH-S-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687286 HCT116-low_APH-S-1 HCT116-low_APH-S-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868419 HCT116-low_APH-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687287 HCT116-low_APH-G2-1 HCT116-low_APH-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868420 HCT116-low_APH-M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687313 HCT116-low_APH-M-1 HCT116-low_APH-M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868421 HCT116-low_APH-S-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687288 HCT116-low_APH-S-2 HCT116-low_APH-S-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868422 HCT116-low_APH-G2-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687317 HCT116-low_APH-G2-2 HCT116-low_APH-G2-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868423 HCT116-low_APH-M-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687289 HCT116-low_APH-M-2 HCT116-low_APH-M-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868424 HCT116-S-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687320 HCT116-S-2 HCT116-S-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868425 HCT116-G2-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687293 HCT116-G2-2 HCT116-G2-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868426 HCT116-M-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687294 HCT116-M-2 HCT116-M-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868427 GM12878-low_APH-RO3306-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687323 GM12878-low_APH-RO3306-G2-1 GM12878-low_APH-RO3306-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868428 HCT116-low_APH-S-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687326 HCT116-low_APH-S-3 HCT116-low_APH-S-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868429 HCT116-low_APH-G2-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687298 HCT116-low_APH-G2-3 HCT116-low_APH-G2-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868430 HCT116-low_APH-S-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687296 HCT116-low_APH-S-4 HCT116-low_APH-S-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868431 HCT116-low_APH-G2-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687297 HCT116-low_APH-G2-4 HCT116-low_APH-G2-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868432 HCT116-low_APH-M-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687325 HCT116-low_APH-M-3 HCT116-low_APH-M-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868433 HCT116-low_APH-RO3306-release-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687302 HCT116-low_APH-RO3306-release-G2-1 HCT116-low_APH-RO3306-release-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868434 HCT116-low_APH-RO3306-release-M-8 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687305 HCT116-low_APH-RO3306-release-M-8 HCT116-low_APH-RO3306-release-M-8 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868435 HCT116-low_APH-RO3306-release-G2-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687306 HCT116-low_APH-RO3306-release-G2-2 HCT116-low_APH-RO3306-release-G2-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868436 HCT116-low_APH-RO3306-release-M-9 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687307 HCT116-low_APH-RO3306-release-M-9 HCT116-low_APH-RO3306-release-M-9 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868437 HCT116-RO3306-release-M-5 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687308 HCT116-RO3306-release-M-5 HCT116-RO3306-release-M-5 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868438 HCT116-low_APH-RO3306-release-M-5 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687333 HCT116-low_APH-RO3306-release-M-5 HCT116-low_APH-RO3306-release-M-5 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868439 HCT116-low_APH-RO3306-release-M-11 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687335 HCT116-low_APH-RO3306-release-M-11 HCT116-low_APH-RO3306-release-M-11 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868440 HCT116-low_APH-RO3306-release-M-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687311 HCT116-low_APH-RO3306-release-M-NU7441-1 HCT116-low_APH-RO3306-release-M-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868441 HCT116-low_APH-RO3306-release-M-ART558-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687334 HCT116-low_APH-RO3306-release-M-ART558-NU7441-1 HCT116-low_APH-RO3306-release-M-ART558-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868442 HCT116-low_APH-RO3306-release-M-POLQ-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687312 HCT116-low_APH-RO3306-release-M-POLQ-1 HCT116-low_APH-RO3306-release-M-POLQ-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868443 HCT116-low_APH-RO3306-release-M-12 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687314 HCT116-low_APH-RO3306-release-M-12 HCT116-low_APH-RO3306-release-M-12 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868444 HCT116-low_APH-RO3306-release-M-ART558-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687332 HCT116-low_APH-RO3306-release-M-ART558-4 HCT116-low_APH-RO3306-release-M-ART558-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868445 HCT116-low_APH-RO3306-release-M-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687316 HCT116-low_APH-RO3306-release-M-NU7441-2 HCT116-low_APH-RO3306-release-M-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868446 HCT116-low_APH-RO3306-release-M-ART558-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687315 HCT116-low_APH-RO3306-release-M-ART558-NU7441-2 HCT116-low_APH-RO3306-release-M-ART558-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868447 HCT116-low_APH-RO3306-release-M-POLQ-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687342 HCT116-low_APH-RO3306-release-M-POLQ-2 HCT116-low_APH-RO3306-release-M-POLQ-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868448 HCT116-low_APH-RO3306-release-M-POLQ-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687337 HCT116-low_APH-RO3306-release-M-POLQ-NU7441-2 HCT116-low_APH-RO3306-release-M-POLQ-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868449 HCT116-RO3306-G2-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687345 HCT116-RO3306-G2-4 HCT116-RO3306-G2-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868450 HCT116-low_APH-RO3306-G2-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687346 HCT116-low_APH-RO3306-G2-3 HCT116-low_APH-RO3306-G2-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868451 HCT116-RO3306-release-M-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687318 HCT116-RO3306-release-M-4 HCT116-RO3306-release-M-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868452 HCT116-RO3306-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687319 HCT116-RO3306-G2-1 HCT116-RO3306-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868453 HCT116-low_APH-RO3306-release-M-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687321 HCT116-low_APH-RO3306-release-M-4 HCT116-low_APH-RO3306-release-M-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868454 HCT116-RO3306-release-M-high_APH_M-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687344 HCT116-RO3306-release-M-high_APH_M-2 HCT116-RO3306-release-M-high_APH_M-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868455 HCT116-low_APH-RO3306-release-M-high_APH_M-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687324 HCT116-low_APH-RO3306-release-M-high_APH_M-2 HCT116-low_APH-RO3306-release-M-high_APH_M-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868456 HCT116-RO3306-G2-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687322 HCT116-RO3306-G2-3 HCT116-RO3306-G2-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868457 HCT116-low_APH-RO3306-G2-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687349 HCT116-low_APH-RO3306-G2-2 HCT116-low_APH-RO3306-G2-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868458 HCT116-RO3306-G2-NVB-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687327 HCT116-RO3306-G2-NVB-1 HCT116-RO3306-G2-NVB-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868459 HCT116-low_APH-RO3306-G2-NVB-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687354 HCT116-low_APH-RO3306-G2-NVB-1 HCT116-low_APH-RO3306-G2-NVB-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868460 HCT116-RO3306-release-M-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687329 HCT116-RO3306-release-M-3 HCT116-RO3306-release-M-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868461 HCT116-low_APH-RO3306-release-M-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687328 HCT116-low_APH-RO3306-release-M-3 HCT116-low_APH-RO3306-release-M-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868462 HCT116-RO3306-release-M-NVB-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687331 HCT116-RO3306-release-M-NVB-1 HCT116-RO3306-release-M-NVB-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868463 HCT116-RO3306-release-M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687330 HCT116-RO3306-release-M-1 HCT116-RO3306-release-M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868464 HCT116-low_APH-RO3306-release-M-NVB-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687357 HCT116-low_APH-RO3306-release-M-NVB-1 HCT116-low_APH-RO3306-release-M-NVB-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868465 HCT116-low_APH-RO3306-S-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687362 HCT116-low_APH-RO3306-S-1 HCT116-low_APH-RO3306-S-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868466 HCT116-low_APH-RO3306-G2 -1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687336 HCT116-low_APH-RO3306-G2 -1 HCT116-low_APH-RO3306-G2 -1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868467 HCT116-low_APH-RO3306-release-M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687338 HCT116-low_APH-RO3306-release-M-1 HCT116-low_APH-RO3306-release-M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868468 HCT116-RO3306-G2-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687341 HCT116-RO3306-G2-2 HCT116-RO3306-G2-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868469 HCT116-low_APH-M-4 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687340 HCT116-low_APH-M-4 HCT116-low_APH-M-4 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868470 HCT116-S-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687339 HCT116-S-3 HCT116-S-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868471 HCT116-low_APH-S-5 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687364 HCT116-low_APH-S-5 HCT116-low_APH-S-5 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868472 HCT116-low_APH-S-LIG4-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687365 HCT116-low_APH-S-LIG4-1 HCT116-low_APH-S-LIG4-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868473 HCT116-low_APH-S-LIG4-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687361 HCT116-low_APH-S-LIG4-ART558-1 HCT116-low_APH-S-LIG4-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868474 GM12878-RO3306-release-M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687343 GM12878-RO3306-release-M-1 GM12878-RO3306-release-M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868475 HCT116-low_APH-S-LIG4-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687347 HCT116-low_APH-S-LIG4-2 HCT116-low_APH-S-LIG4-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868476 HCT116-low_APH-S-LIG4-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687371 HCT116-low_APH-S-LIG4-ART558-2 HCT116-low_APH-S-LIG4-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868477 HCT116-low_APH-S-POLQ-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687348 HCT116-low_APH-S-POLQ-1 HCT116-low_APH-S-POLQ-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868478 HCT116-low_APH-S-POLQ-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687352 HCT116-low_APH-S-POLQ-NU7441-1 HCT116-low_APH-S-POLQ-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868479 HCT116-low_APH-S-POLQ-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687350 HCT116-low_APH-S-POLQ-2 HCT116-low_APH-S-POLQ-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868480 HCT116-low_APH-S-POLQ-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687351 HCT116-low_APH-S-POLQ-NU7441-2 HCT116-low_APH-S-POLQ-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868481 HCT116-low_APH-3 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687353 HCT116-low_APH-3 HCT116-low_APH-3 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868482 HCT116-low_APH-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687367 HCT116-low_APH-ART558-2 HCT116-low_APH-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868483 HCT116-low_APH-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687369 HCT116-low_APH-NU7441-2 HCT116-low_APH-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868484 HCT116-low_APH-ART558-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687370 HCT116-low_APH-ART558-NU7441-2 HCT116-low_APH-ART558-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868485 GM12878-low_APH-RO3306-release-M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687378 GM12878-low_APH-RO3306-release-M-1 GM12878-low_APH-RO3306-release-M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868486 HCT116-low_APH-LIG4-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687372 HCT116-low_APH-LIG4-1 HCT116-low_APH-LIG4-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868487 HCT116-low_APH-LIG4-ART558-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687356 HCT116-low_APH-LIG4-ART558-1 HCT116-low_APH-LIG4-ART558-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868488 HCT116-low_APH-LIG4-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687355 HCT116-low_APH-LIG4-2 HCT116-low_APH-LIG4-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868489 HCT116-low_APH-LIG4-ART558-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687358 HCT116-low_APH-LIG4-ART558-2 HCT116-low_APH-LIG4-ART558-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868490 HCT116-low_APH-POLQ-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687376 HCT116-low_APH-POLQ-1 HCT116-low_APH-POLQ-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868491 HCT116-low_APH-POLQ-NU7441-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687359 HCT116-low_APH-POLQ-NU7441-1 HCT116-low_APH-POLQ-NU7441-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868492 HCT116-low_APH-POLQ-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687360 HCT116-low_APH-POLQ-2 HCT116-low_APH-POLQ-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868493 HCT116-low_APH-POLQ-NU7441-2 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687363 HCT116-low_APH-POLQ-NU7441-2 HCT116-low_APH-POLQ-NU7441-2 WGS GENOMIC Hybrid Selection Illumina NovaSeq X Plus SRX23868494 HCT116-RO3306-release-G2-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687380 HCT116-RO3306-release-G2-1 HCT116-RO3306-release-G2-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868495 HCT116-RO3306-release-M-8 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line HCT116 SRS20687382 HCT116-RO3306-release-M-8 HCT116-RO3306-release-M-8 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000 SRX23868496 GM12878-RO3306-release-M-high_APH_M-1 SRP493858 bp0 svCapture WGS for common fragile sites applied to variably treated samples of cell line GM12878 SRS20687366 GM12878-RO3306-release-M-high_APH_M-1 GM12878-RO3306-release-M-high_APH_M-1 WGS GENOMIC Hybrid Selection Illumina NovaSeq 6000