Figure S1. Vectorette PCR amplicons quality control. a. Electrophoresis of vectorette PCR amplicons. The gel image shows five lanes: [L] 2-log ladder (NEB) [1], 2 μg purified PCR amplicons [2], 2 μg purified PCR amplicons digested with BstYI [3], 2 μg purified PCR amplicons ‘contaminated’ with concatemers [4], 2 μg purified PCR amplicons digested with BstYI showing concatemer band at ~ 50 bp. A good vectorette PCR will present as a smear of amplicons averaging 1-3 kb (lane 1). A very high molecular weight smear could indicate contamination (lane 3). b. Schematic of possible vectorette-primer concatemer. Digestion of the amplicons with BstYI, which cuts inside the vectorette primer sequence, will produce a visible band at ~ 50 bp if concatem...
Table S1. Mutagenesis, amplification and sequencing primers in the plasmid system. Amplification/seq...
Table S1. PCR#1 primer sequences for amplification of bisulfite-converted genomic DNA. Forward and r...
Figure S7. UDiTaS characterization of plasmid standards without carrier DNA. To ensure that the carr...
Figure S2. DNA size distributions during TIPseq. a. An Agilent TapeStation image of two samples of p...
Primer pairs used in PCR. Figure S1. Circular map of T-DNA construct. Figure S2. PCR confirmation of...
Figure S1. Gel electrophoresis of amplification products in TAIL-PCR. Figure S2. Gel electrophoresis...
Table S1. Target sequences within the CCR5 gene of engineered nucleases. Table S2. Primers used for ...
Normalization of tagmentation activity based on pre-PCR insertion size distribution. Activity is nor...
Figure S2. The detection of two potential breakpoints by agarose gel electrophoresis. PCR amplificat...
Figure S5. Genome mapping rates for UDiTaS. Individual reads map to the expected genome site with hi...
Figure S6. UDiTaS characterization and comparison to AMP-Seq with plasmid standards. Plasmids contai...
Six patterns of amplicons are repeatedly identified from multiple Sp185/333-positive BAC clones. A. ...
Depth of unique coverage according to the size of the target regions (x-axis). Target regions adjace...
DNA binding stability of Tn5 vs. Tn5-059. While heating at 74.2 °C is required for Tn5 to dissociate...
Figure S1. Pulsed field gel electrophoresis image of B73 high molecular weight DNA after extraction ...
Table S1. Mutagenesis, amplification and sequencing primers in the plasmid system. Amplification/seq...
Table S1. PCR#1 primer sequences for amplification of bisulfite-converted genomic DNA. Forward and r...
Figure S7. UDiTaS characterization of plasmid standards without carrier DNA. To ensure that the carr...
Figure S2. DNA size distributions during TIPseq. a. An Agilent TapeStation image of two samples of p...
Primer pairs used in PCR. Figure S1. Circular map of T-DNA construct. Figure S2. PCR confirmation of...
Figure S1. Gel electrophoresis of amplification products in TAIL-PCR. Figure S2. Gel electrophoresis...
Table S1. Target sequences within the CCR5 gene of engineered nucleases. Table S2. Primers used for ...
Normalization of tagmentation activity based on pre-PCR insertion size distribution. Activity is nor...
Figure S2. The detection of two potential breakpoints by agarose gel electrophoresis. PCR amplificat...
Figure S5. Genome mapping rates for UDiTaS. Individual reads map to the expected genome site with hi...
Figure S6. UDiTaS characterization and comparison to AMP-Seq with plasmid standards. Plasmids contai...
Six patterns of amplicons are repeatedly identified from multiple Sp185/333-positive BAC clones. A. ...
Depth of unique coverage according to the size of the target regions (x-axis). Target regions adjace...
DNA binding stability of Tn5 vs. Tn5-059. While heating at 74.2 °C is required for Tn5 to dissociate...
Figure S1. Pulsed field gel electrophoresis image of B73 high molecular weight DNA after extraction ...
Table S1. Mutagenesis, amplification and sequencing primers in the plasmid system. Amplification/seq...
Table S1. PCR#1 primer sequences for amplification of bisulfite-converted genomic DNA. Forward and r...
Figure S7. UDiTaS characterization of plasmid standards without carrier DNA. To ensure that the carr...